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FDA Inspection
•Bora Pharmaceuticals Laboratories, Inc•July 21, 2025

Bora Pharmaceuticals Laboratories, Inc – FDA Inspection, Jul 21, 2025

Record Details

This FDA Inspection record concerns Bora Pharmaceuticals Laboratories, Inc, with an inspection on July 21, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Bora Pharmaceuticals Laboratories, Inc
Inspection Date
July 21, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Brandy N. Lepage (FDA Associated Person)
View Company Profile

ID · 3971468c-f04b-41d5-9b6a-f3926d7a8206

Inspection Facts

Inspection number
1273032
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Bora Pharmaceuticals Laboratories, Inc

6
DateClassificationOfficeProject area
May 24, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 17, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 15, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 26, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 26, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Bora Pharmaceuticals Laboratories, Inc
  • FDA Inspection 1095577 - 2019-05-24
  • FDA Inspection 1008321 - 2017-02-17
  • FDA Inspection 971066 - 2016-04-15
  • FDA Inspection 890281 - 2014-07-26
  • FDA Inspection 797513 - 2012-07-26

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