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FDA Inspection
•Sidmak Laboratories India Pvt Ltd•May 13, 2023

Sidmak Laboratories India Pvt Ltd – FDA Inspection, May 13, 2023

Record Details

This FDA Inspection record concerns Sidmak Laboratories India Pvt Ltd, with an inspection on May 13, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Sidmak Laboratories India Pvt Ltd
Inspection Date
May 13, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Dipesh K. Shah
View Company Profile

ID · 3c2aa7e8-0d61-412b-beb5-0209a78665d3

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1207996
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Sidmak Laboratories India Pvt Ltd

5
DateClassificationOfficeProject area
February 14, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 6, 2019OAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
March 31, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 6, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 26, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Sidmak Laboratories India Pvt Ltd
  • FDA Inspection 1123559 - 2020-02-14
  • FDA Inspection 1102227 - 2019-09-06
  • FDA Inspection 1009631 - 2017-03-31
  • FDA Inspection 881291 - 2014-06-06
  • FDA Inspection 806835 - 2012-10-26

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