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FDA Inspection
•Unichem Laboratories Limited•March 20, 2017

Unichem Laboratories Limited – FDA Inspection, Mar 20, 2017

Record Details

This FDA Inspection record concerns Unichem Laboratories Limited, with an inspection on March 20, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Unichem Laboratories Limited
Inspection Date
March 20, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Daniel J. Roberts (FDA Associated Person)
  • Mathew T. Thomas (Issuing Officer)
View Company Profile

ID · 07453729-374b-428c-8b1c-e74e214fdf05

Inspection Facts

Inspection number
1009098
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Unichem Laboratories Limited

7
DateClassificationOfficeProject area
September 26, 2026Not classifiedOffice of Inspections and Investigations
July 15, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 12, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 31, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 17, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Unichem Laboratories Limited
  • FDA Inspection 1337024 - 2026-09-26
  • FDA Inspection 1243288 - 2024-07-15
  • FDA Inspection 1159456 - 2020-01-12
  • FDA Inspection 1102049 - 2019-07-31
  • FDA Inspection 922923 - 2015-04-17

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