# FDA Inspection 1277747 - Eurofins Biopharma Product Testing Munich GmbH - June 23, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/5980c290-e543-4bd9-9b68-c20ada20e1be
Source feed: FDA_Inspections

> FDA Inspection 1277747 for Eurofins Biopharma Product Testing Munich GmbH on June 23, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1277747
- Company Name: Eurofins Biopharma Product Testing Munich GmbH
- Inspection Date: 2023-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1096402 - 2019-07-12](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/795f6535-fb07-42ad-96bc-0a5046cb23fd)
- [FDA Inspection 895118 - 2014-09-12](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/4c158ee2-c7d0-4e23-b068-f4df75541c7f)

Company: https://www.globalkeysolutions.net/companies/eurofins-biopharma-product-testing-munich-gmbh/e6b00a51-7e13-4203-8500-8f3e177a1a99

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c