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FDA Inspection
•Recipharm Pharmaservices Private Limited•December 14, 2017

Recipharm Pharmaservices Private Limited – FDA Inspection, Dec 14, 2017

Record Details

This FDA Inspection record concerns Recipharm Pharmaservices Private Limited, with an inspection on December 14, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Recipharm Pharmaservices Private Limited
Inspection Date
December 14, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Kellia N. Hicks (FDA Associated Person)
View Company Profile

ID · 0f338ab7-111a-4a18-a919-9a24011077df

Inspection Facts

Inspection number
1037690
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Recipharm Pharmaservices Private Limited

8
DateClassificationOfficeProject area
March 22, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 13, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 1, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 7, 2018VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
May 11, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Recipharm Pharmaservices Private Limited
  • FDA Inspection 1232473 - 2024-03-22
  • FDA Inspection 1119410 - 2020-02-13
  • FDA Inspection 1079034 - 2019-02-01
  • FDA Inspection 1075220 - 2018-12-07
  • FDA Inspection 1053644 - 2018-05-11

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