# Bristol-Myers Squibb Company - Inspection Records

Source: https://www.globalkeysolutions.net/companies/bristol-myers-squibb-company/be7fcaee-1b54-4e0d-82a3-85d9c545b073

> Inspection records and compliance data for Bristol-Myers Squibb Company in Wallingford, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Bristol-Myers Squibb Company
- FEI Number: 1283703
- City: Wallingford
- State: Connecticut
- Country Name: United States
- Address Line 1: 5 Research Pkwy
- Zip Code: 06492

## Related Documents

- [483 - Bristol-Myers Squibb Company - 2025-07-08](https://www.globalkeysolutions.net/records/483/bristol-myers-squibb-company/cd0235d4-6c95-4411-a362-48e93ec367cb) — source: FDA, date: July 8, 2025
- [FDA Inspection 945016 - Bristol-Myers Squibb Company - 2015-09-17](https://www.globalkeysolutions.net/records/fda_inspections/bristol-myers-squibb-company/3f61c051-38ce-4d6b-b0f2-42036c788c13) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2015
- [FDA Inspection 857394 - Bristol-Myers Squibb Company - 2013-11-25](https://www.globalkeysolutions.net/records/fda_inspections/bristol-myers-squibb-company/91143c29-b7f9-4d8d-bf1a-05eeea30b747) — classification: No Action Indicated (NAI), source: FDA, date: November 25, 2013
- [FDA Inspection 812983 - Bristol-Myers Squibb Company - 2012-11-30](https://www.globalkeysolutions.net/records/fda_inspections/bristol-myers-squibb-company/0f78e60d-f4bd-419f-b40c-1411e79f914e) — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2012
- [FDA Inspection 704230 - Bristol-Myers Squibb Company - 2010-12-02](https://www.globalkeysolutions.net/records/fda_inspections/bristol-myers-squibb-company/2ab3b5c6-daf1-4d80-8745-49328b04da64) — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2010
- [FDA Inspection 682482 - Bristol-Myers Squibb Company - 2010-09-14](https://www.globalkeysolutions.net/records/fda_inspections/bristol-myers-squibb-company/bc12d8a0-e573-4892-8c37-ed3a4832f0ca) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2010

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