# Provita Eurotech Ltd. – FDA Inspection, Oct 23, 2014

Source: https://www.keypedia.com/records/fda_inspections/provita-eurotech-ltd/64234a94-0d6c-4fcc-8f2b-a92fbfc432dd
Source feed: FDA_Inspections

> FDA inspection 902031 of Provita Eurotech Ltd., October 23, 2014. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 211. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 902031
- Company Name: Provita Eurotech Ltd.
- Inspection Date: 2014-10-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Monitoring of Marketed Animal Drugs, Feed, and Devices
- Product Type: Veterinary
- Center: Animal Drugs & Feeds
- Office Name: Center for Veterinary Medicine
- Citation Count: 7

## Related Documents

- FDA Inspection 976047 - 2016-06-15

Company: https://www.keypedia.com/companies/provita-eurotech-ltd/232515f3-e830-4192-9609-83fc2a059fea

Office: https://www.keypedia.com/offices/center-for-veterinary-medicine/7e30a309-56e4-4e7a-8b8b-e07674bb07b4