# FDA Inspection 1039985 - Eurofins Dr. Specht International GmbH - February 02, 2018

Source: https://www.keypedia.com/records/fda_inspections/eurofins-dr-specht-international-gmbh/2e7ad322-15a7-41a1-a994-90f9f0aa76a9
Source feed: FDA_Inspections

> FDA Inspection 1039985 for Eurofins Dr. Specht International GmbH on February 02, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039985
- Company Name: Eurofins Dr. Specht International GmbH
- Inspection Date: 2018-02-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 841943 - 2013-07-10](https://www.keypedia.com/records/fda_inspections/eurofins-dr-specht-international-gmbh/1b063d23-24ce-4be0-a633-6e71a632a479)

Company: https://www.keypedia.com/companies/eurofins-dr-specht-international-gmbh/2eb18149-9fdf-4790-881b-911d9d5c3090

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