# Eurofins BioPharma Product Testing Czech Republic s.r.o. – FDA Inspection, Jul 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-czech-republic-sro/cca7e136-ec3b-4624-bca0-a5e63ae6a4d7
Source feed: FDA_Inspections

> FDA inspection 892490 of Eurofins BioPharma Product Testing Czech Republic s.r.o., July 29, 2014. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 211. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 892490
- Company Name: Eurofins BioPharma Product Testing Czech Republic s.r.o.
- Inspection Date: 2014-07-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 4

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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