# FDA Inspection 1091920 - Eurofins Pharma Quality Control - September 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/eurofins-pharma-quality-control/b96b75a3-924b-4bf7-893d-be4b91dade3c
Source feed: FDA_Inspections

> FDA Inspection 1091920 for Eurofins Pharma Quality Control on September 08, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091920
- Company Name: Eurofins Pharma Quality Control
- Inspection Date: 2017-09-08
- Classification: Voluntary Action Indicated (VAI)
- 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-pharma-quality-control/5514c989-045b-4bbe-8c35-91d5f3b7c822

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