# Eurofins Biopharma Product Testing Munich GmbH - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-munich-gmbh/e6b00a51-7e13-4203-8500-8f3e177a1a99

> Inspection records and compliance data for Eurofins Biopharma Product Testing Munich GmbH in Planegg, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Biopharma Product Testing Munich GmbH
- FEI Number: 3003706029
- City: Planegg
- State: None
- Country Name: Germany
- Address Line 1: Robert-Koch-Str. 3a
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1277747 - Eurofins Biopharma Product Testing Munich GmbH - 2023-06-23](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/5980c290-e543-4bd9-9b68-c20ada20e1be) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 23, 2023
- [483 - Eurofins Biopharma Product Testing Munich GmbH - 2019-07-12](https://www.keypedia.com/records/483/eurofins-biopharma-product-testing-munich-gmbh/99c0ec8a-914c-43c9-944a-879640079953) — source: FDA, date: July 12, 2019
- [FDA Inspection 1096402 - Eurofins Biopharma Product Testing Munich GmbH - 2019-07-12](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/795f6535-fb07-42ad-96bc-0a5046cb23fd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2019
- [FDA Inspection 895118 - Eurofins Biopharma Product Testing Munich GmbH - 2014-09-12](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-munich-gmbh/4c158ee2-c7d0-4e23-b068-f4df75541c7f) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2014

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## Related Officers

- [Compliance Officer - CDER/OC/OMQ](https://www.keypedia.com/people/anita-narula/fbebf5a2-e25c-4e98-9c22-433d9102380c)