# VRL Eurofins – FDA Inspection, Oct 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/vrl-eurofins/df00af64-ef74-466d-a350-c3c328eeb075
Source feed: FDA_Inspections

> FDA inspection 901718 of VRL Eurofins, October 29, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 1271. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901718
- Company Name: VRL Eurofins
- Inspection Date: 2014-10-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 1

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Company: https://www.keypedia.com/companies/vrl-eurofins/50158b01-810a-402a-8a30-e8b7021b8b3f

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d