# AmerisourceBergen Drug Corp. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/amerisourcebergen-drug-corp/e20bdc98-7510-4048-86b3-df5aa0932d27

> Inspection records and compliance data for AmerisourceBergen Drug Corp. in Morrisville, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: AmerisourceBergen Drug Corp.
- FEI Number: 3007181228
- City: Morrisville
- State: North Carolina
- Country Name: United States
- Address Line 1: 120 Trans Air Dr
- Zip Code: 27560

## Related Documents

- [FDA Inspection 1284394 - AmerisourceBergen Drug Corp. - 2025-09-23](https://www.globalkeysolutions.net/records/fda_inspections/amerisourcebergen-drug-corp/7fd48e4c-2543-49d2-947d-99853b2bf052) — source: FDA, date: September 23, 2025
- [FDA Inspection 1284394 - AmerisourceBergen Drug Corp. - 2025-09-23](https://www.globalkeysolutions.net/records/fda_inspections/amerisourcebergen-drug-corp/d704c9de-2646-4bd5-84bc-4594bc4ba6b1) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2025
- [483 - AmerisourceBergen Drug Corp. - 2023-06-15](https://www.globalkeysolutions.net/records/483/amerisourcebergen-drug-corp/22f5053c-7cde-4780-a772-6a323bfda179) — source: FDA, date: June 15, 2023
- [FDA Inspection 1208142 - AmerisourceBergen Drug Corp. - 2023-06-15](https://www.globalkeysolutions.net/records/fda_inspections/amerisourcebergen-drug-corp/26e7520a-1d50-41c6-9ba3-4239e0577af3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2023
- [FDA Inspection 1208142 - AmerisourceBergen Drug Corp. - 2023-06-15](https://www.globalkeysolutions.net/records/fda_inspections/amerisourcebergen-drug-corp/f65c86c2-aaf7-411c-bc29-8ed7101bb5e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2023
- [FDA Inspection 1001450 - AmerisourceBergen Drug Corp. - 2017-01-17](https://www.globalkeysolutions.net/records/fda_inspections/amerisourcebergen-drug-corp/fc357058-a4d7-4127-9634-8cc3747fffea) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2017

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