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FDA Inspection
•Sri Krishna Pharmaceuticals, Ltd. - Unit III•July 31, 2023

Sri Krishna Pharmaceuticals, Ltd. - Unit III – FDA Inspection, Jul 31, 2023

Record Details

This FDA Inspection record concerns Sri Krishna Pharmaceuticals, Ltd. - Unit III, with an inspection on July 31, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Sri Krishna Pharmaceuticals, Ltd. - Unit III
Inspection Date
July 31, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Sandra A. Boyd (Investigator)
  • Vaishali J. Patel
View Company Profile

ID · bfd65ca0-6288-4752-be58-bf323fa42b5c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1216334
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Sri Krishna Pharmaceuticals, Ltd. - Unit III

2
DateClassificationOfficeProject area
October 23, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 25, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Sri Krishna Pharmaceuticals, Ltd. - Unit III
  • FDA Inspection 954833 - 2015-10-23
  • FDA Inspection 757343 - 2011-11-25

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