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FDA Inspection
•LEESAR, INC•September 23, 2026

LEESAR, INC – FDA Inspection, Sep 23, 2026

Record Details

This FDA Inspection record concerns LEESAR, INC, with an inspection on September 23, 2026, issued by the Florida District Office, covering human drugs.

Company
LEESAR, INC
Inspection Date
September 23, 2026
Product Type
Human Drugs
Office
Florida District Office
People
  • Jonathan G. Matrisciano (FDA Associated Person)
  • Kayla V. Sprague (FDA Associated Person)
View Company Profile

ID · e4951ec0-3f11-4759-94f5-93eaf99c3861

Inspection Facts

Inspection number
1337198
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of LEESAR, INC

5
DateClassificationOfficeProject area
July 18, 2025NAIFlorida District OfficePostmarket Assurance: Medical Devices
May 9, 2025VAIFlorida District OfficeDrug Quality Assurance
October 29, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 12, 2017OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 8, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for LEESAR, INC
  • FDA Inspection 1276435 - 2025-07-18
  • FDA Inspection 1269588 - 2025-05-09
  • FDA Inspection 1155647 - 2021-10-29
  • FDA Inspection 1017863 - 2017-07-12
  • FDA Inspection 893985 - 2014-08-08

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