FDA Inspection
Bristol-Myers Squibb CompanyBristol-Myers Squibb Company – FDA Inspection, Mar 19, 2010
Record Details
This FDA Inspection record concerns Bristol-Myers Squibb Company, with an inspection on March 19, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Bristol-Myers Squibb Company
- Inspection Date
- March 19, 2010
- Product Type
- Drugs
View Company Profile
ID · 37d064a2-3437-452a-aaf9-5600679a344a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 653973
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.165(d)Acceptance criteria for sampling & testing
- 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
- 21 CFR 211.180(e)Records reviewed annually
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Bristol-Myers Squibb Company
16| Date | Classification | Office | Project area |
|---|---|---|---|
| June 23, 2026 | Not classified | New Jersey District Office | |
| July 18, 2025 | Not classified | New Jersey District Office | |
| December 6, 2024 | VAI | New Jersey District Office | Postmarketing Surveillance and Epidemiology: Human Drugs |
| September 6, 2024 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| January 31, 2024 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
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