# Eurofins BioPharma Product Testing Hamburg GmbH – FDA Inspection, Jul 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-hamburg-gmbh/32d370fa-6547-4426-ba48-4931d6e2e9c9
Source feed: FDA_Inspections

> FDA inspection 841999 of Eurofins BioPharma Product Testing Hamburg GmbH, July 10, 2013. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 841999
- Company Name: Eurofins BioPharma Product Testing Hamburg GmbH
- Inspection Date: 2013-07-10
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1288412 - 2022-10-19
- FDA Inspection 1109935 - 2019-09-18

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

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