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FDA Inspection
•Piramal Pharma Limited•February 21, 2017

Piramal Pharma Limited – FDA Inspection, Feb 21, 2017

Record Details

This FDA Inspection record concerns Piramal Pharma Limited, with an inspection on February 21, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Piramal Pharma Limited
Inspection Date
February 21, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Daniel J. Roberts (FDA Associated Person)
  • Paula Katz (Issuing Officer)
View Company Profile

ID · 4d5108d6-21cc-4fe9-b32e-d5c82096ac34

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1005197
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Piramal Pharma Limited

8
DateClassificationOfficeProject area
May 19, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 30, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 18, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 30, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
April 3, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Piramal Pharma Limited
  • FDA Inspection 1208559 - 2023-05-19
  • FDA Inspection 1103288 - 2019-08-30
  • FDA Inspection 1081925 - 2019-01-18
  • FDA Inspection 951067 - 2015-10-30
  • FDA Inspection 924411 - 2015-04-03

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