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FDA Inspection
•Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company•September 11, 2017

Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company – FDA Inspection, Sep 11, 2017

Record Details

This FDA Inspection record concerns Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company, with an inspection on September 11, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company
Inspection Date
September 11, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Ivis L. Negron Torres (Issuing Officer)
  • Libia M. Lugo (Issuing Officer)
  • Noreen Muniz (FDA Associated Person)
View Company Profile

ID · 1650c515-0cbd-4eb9-82f5-f588c5791f89

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1030016
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company

13
DateClassificationOfficeProject area
February 13, 2026Not classifiedSan Juan District Office
June 6, 2024Not classifiedSan Juan District Office
July 12, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 19, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 6, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 13 other inspections on the company page
Other documents for Bristol-Myers Squibb Holdings Pharma Ltd. Liability Company
  • FDA Inspection 1305236 - 2026-02-13
  • FDA Inspection 1242629 - 2024-06-06
  • FDA Inspection 1147009 - 2021-07-12
  • FDA Inspection 1110480 - 2019-11-19
  • FDA Inspection 1079769 - 2019-02-06

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