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FDA register as of 2026-10-13 · Compiled and edited by

Leesar Inc.

Leesar Inc., Fort Myers, FL, is registered with the FDA as a 503B outsourcing facility (first registered 4/30/2014; most recent registration 11/26/2025). The FDA last inspected it on 9/28/2026; a Form 483 was issued, a recall was not conducted, and the action recorded is “Open”.

Status
503B REGISTERED
Location
Fort Myers, FL
First registration
4/30/2014
Most recent registration
11/26/2025
Last FDA inspection
9/28/2026
Form 483 issued
Yes
Recall conducted
No
Action based on last inspection
Open
Compounds sterile drugs from bulk
No
Contact listed by the FDA
Maria Gautier · 1-239-939-8925

Florida pharmacy permits

Florida Department of Health, Division of Medical Quality Assurance (Board of Pharmacy) · data as of 2026-10-15

Permit
PH31810 · board record
Status
CLEAR
Qualifications (board's wording)
Special Sterile Compounding · Outsourcing Facility
Trade name on permit
SOUTHWEST FLORIDA PHARMACEUTICAL REPACK
Permit holder
LEESAR INC.
Original issue date
12/21/2018
Expiration date
2/28/2027
Address of record
2727 WINKLER AVE
FT MYERS, FL 33901
Discipline on file
No
Public complaint
No

Qualifications are the lines the board prints on each permit page, reproduced as printed; this site adds no permit type of its own. Permits this pharmacy may hold in other states are not shown here yet.

Every FDA-registered 503B facility in Florida, with its state permit: Florida outsourcing facility permits.

How to read these fields

The board defines the two flags itself. On “Public Complaint”:

A public complaint (administrative complaint) is not disciplinary action. It is a charging document that has not been proven. A public administrative complaint is the result of a complaint and the investigation of the allegation of a violation of the practice act that governs a health care profession. The administrative complaint lists the violations of law that were alleged after the investigation and review that resulted in a finding of probable cause.

Source: Florida DOH MQA, License Verification, “Public Complaint Definition”, read 2026-10-15.

And on how a complaint becomes “Discipline on File”:

Some public administrative complaints are dismissed at the hearing stage. Other administrative complaints result in disciplinary action imposed by a final order, which is reflected as a “YES” in the “Discipline on File” entry on the licensee verification screen.

Source: Florida DOH MQA, License Verification, “Public Complaint Definition”, read 2026-10-15.

Source: Florida Department of Health, Division of Medical Quality Assurance (Board of Pharmacy), License Verification (search), each permit's page read at build with the board's “Data As Of” 2026-10-15; cross-checked against the board's bulk export of 27,177 Board of Pharmacy permits downloaded 2026-10-15. Status wording is the board's.

This facility's row on the FDA list changed in September 2026. What changed: 503B register changes.

How to read this record

Registration means the facility has registered with the FDA under section 503B and is subject to FDA inspection under current good manufacturing practice. It is not an endorsement. A Form 483 is the list of observations an investigator leaves at the end of an inspection; it is not a finding of violation, and most inspected facilities on the register have received one. “Open” means the FDA has not finalised the inspection's classification. A regulatory meeting or a warning letter is a further step, and the FDA posts the letter, which we link when it does.

What this page does not tell you: whether a specific drug from this facility is right for you, or whether the telehealth brand that sold it to you is the same entity. Compounded prescriptions are labelled with the pharmacy that made them — compare that label to this name.

Other registered facilities in Florida

The FDA lists 15 registered 503B facilities in Florida. Their records, and the state's 503A pharmacies: compounding pharmacies in Florida.

Source: FDA — Registered Outsourcing Facilities, as of 2026-10-13; every value above is the FDA's, reproduced without characterisation. Back to the full register, or look up another pharmacy.

Before you sign

Is this the name on your label?

If it isn't, look that one up — and if it is a state-licensed 503A pharmacy, we'll point you to the board that holds its license.

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Three checks before you sign

  1. Find the pharmacy on the label. Compounded drugs name the pharmacy that made them, not the telehealth brand that sold them. That name is what you look up.

  2. Read the public record. Whether it is an FDA-registered 503B facility or a state-licensed 503A pharmacy, when it was last inspected, and what the FDA wrote down.

  3. Compare the approved path. What the FDA-approved version costs today next to the compounded one, and which licensed providers prescribe it — so the choice is yours, made on the record.

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