# FDA Inspection 988104 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - August 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-czech-republic-sro/c3e2c10c-50e5-4a31-be1d-0954bd2f1035
Source feed: FDA_Inspections

> FDA Inspection 988104 for Eurofins BioPharma Product Testing Czech Republic s.r.o. on August 09, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988104
- Company Name: Eurofins BioPharma Product Testing Czech Republic s.r.o.
- Inspection Date: 2016-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-czech-republic-sro/2d5e4f85-9d30-4abf-b019-3129dbffe3ca

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