FDA Inspection
Provita Eurotech Ltd.Provita Eurotech Ltd. – FDA Inspection, Oct 23, 2014
Record Details
This FDA Inspection record concerns Provita Eurotech Ltd., with an inspection on October 23, 2014, issued by the Center for Veterinary Medicine, covering veterinary.
- Company
- Provita Eurotech Ltd.
- Inspection Date
- October 23, 2014
- Product Type
- Veterinary
View Company Profile
ID · 64234a94-0d6c-4fcc-8f2b-a92fbfc432dd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 902031
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
FDA Citations
7- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.160(b)(1)Incoming lots - conformance to written specs-
- 21 CFR 211.165(a)Testing and release for distribution
- 21 CFR 211.160(a)Lab controls established, including changes
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Provita Eurotech Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2016 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Provita Eurotech Ltd.
- FDA Inspection 976047 - 2016-06-15
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