# Bristol-Myers Squibb Company – FDA 483, Jun 16, 2023

Source: https://www.keypedia.com/records/483/bristol-myers-squibb-company/4ea843bb-7d44-433b-b1f8-807afaf7865e

> FDA 483 for Bristol-Myers Squibb Company on June 16, 2023. Product: biologics. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Bristol-Myers Squibb Company
- Inspection Date: 2023-06-16
- Product Type: biologics
- Office Name: New Jersey District Office
- Summary: Celgene Corporation in Summit, NJ, a licensed biological drug manufacturer, was cited for significant deficiencies during an FDA inspection. The observations include a lack of appropriate stability data for drug product expiration dating and inadequate validated procedures for visual inspection of Abecma. Furthermore, the firm's aseptic processing areas showed critical failures in environmental and personnel monitoring, alongside facility design issues that could compromise contamination control.

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## Related Officers

- [Director, Team Biologics Staff](https://www.keypedia.com/people/helen-b-ricalde/455f022e-4d32-453e-acc7-e84a53ce730c)
- [issuing_officer](https://www.keypedia.com/people/emily-a-walters/e80b3581-ffba-4244-9030-b6c9496da932)
- [Investigator](https://www.keypedia.com/people/unnee-ranjan/43f1d07e-4079-4d33-88a9-baf6a5df932c)

Company: https://www.keypedia.com/companies/bristol-myers-squibb-company/3734a119-014f-49c6-b518-fc8b1dea7f92

Office: https://www.keypedia.com/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248