FDA Inspection
Tenda Horse Products LLCTenda Horse Products LLC – FDA Inspection, Dec 21, 2010
Record Details
This FDA Inspection record concerns Tenda Horse Products LLC, with an inspection on December 21, 2010, issued by the Center for Veterinary Medicine, covering veterinary.
- Company
- Tenda Horse Products LLC
- Inspection Date
- December 21, 2010
- Product Type
- Veterinary
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ID · 7089c90d-c277-464b-b0ea-d92af2362582
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 702921
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
FDA Citations
8- 21 CFR 211.65(a)Equipment construction - reactive surfaces
- 21 CFR 211.125(d)Destruction of excess labels with lot numbers
- 21 CFR 211.113(a)Procedures for non-sterile drug products
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.165(a)Testing and release for distribution
- 21 CFR 211.166(a)Lack of written stability program
- 21 CFR 211.180(e)(2)Items to cover on annual reviews
- 21 CFR 211.67(b)Written procedures fail to include
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Tenda Horse Products LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 17, 2024 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| August 9, 2018 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| July 10, 2015 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| December 20, 2012 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| July 31, 2009 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Tenda Horse Products LLC
- FDA Inspection 1238775 - 2024-05-17
- FDA Inspection 1063489 - 2018-08-09
- FDA Inspection 933990 - 2015-07-10
- FDA Inspection 811379 - 2012-12-20
- FDA Inspection 600912 - 2009-07-31
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