FDA Inspection
S&A Kreider & SonsS&A Kreider & Sons – FDA Inspection, Nov 1, 2017
Record Details
This FDA Inspection record concerns S&A Kreider & Sons, with an inspection on November 1, 2017, issued by the Center for Veterinary Medicine, covering veterinary.
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ID · 6f06a6b9-2207-41de-8758-f8a0aa82afa6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030431
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 530.11(d)ELDU - producer causes Illegal drug residue
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Other FDA inspections of S&A Kreider & Sons
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 24, 2021 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| February 22, 2017 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for S&A Kreider & Sons
- FDA Inspection 1157733 - 2021-11-24
- FDA Inspection 1009755 - 2017-02-22
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