# Eurofins BioPharma Product Testing Hamburg GmbH - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-hamburg-gmbh/9bd1a192-5cc1-4d70-a56d-850a0a686451

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

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## Details

- Name: Eurofins BioPharma Product Testing Hamburg GmbH
- FEI Number: 3010166293
- City: Hamburg
- State: None
- Country Name: Germany
- Address Line 1: Am Neulander Gewerbepark 2
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1288412 - Eurofins BioPharma Product Testing Hamburg GmbH - 2022-10-19](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-hamburg-gmbh/f1bba640-ba6e-42ae-94b1-5cf2bea9b08e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2022
- [FDA Inspection 1109935 - Eurofins BioPharma Product Testing Hamburg GmbH - 2019-09-18](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-hamburg-gmbh/765a3cdb-eedb-414d-b235-a071ca81f3ac) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2019
- [FDA Inspection 841999 - Eurofins BioPharma Product Testing Hamburg GmbH - 2013-07-10](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-hamburg-gmbh/32d370fa-6547-4426-ba48-4931d6e2e9c9) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2013

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