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FDA Inspection
•Kaytee Products, Inc.•February 14, 2023

Kaytee Products, Inc. – FDA Inspection, Feb 14, 2023

Record Details

This FDA Inspection record concerns Kaytee Products, Inc., with an inspection on February 14, 2023, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Kaytee Products, Inc.
Inspection Date
February 14, 2023
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Rebecca L. Mullikin (Investigator)
View Company Profile

ID · 6394d6c7-0507-40d0-b5e6-6460865e1326

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1197593
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

FDA Citations

6
  1. 21 CFR 507.40(c)(1)Monitoring Records for Preventive Controls
  2. 21 CFR 507.33(a)Hazard Analysis
  3. 21 CFR 507.47(a)Validation of Process or Other Preventive Control
  4. 21 CFR 507.33(a)Hazard Analysis
  5. 21 CFR 507.40(c)(1)Monitoring Records for Preventive Controls
  6. 21 CFR 507.47(a)Validation of Process or Other Preventive Control

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kaytee Products, Inc.

7
DateClassificationOfficeProject area
September 11, 2025Not classifiedMinneapolis District Office
November 30, 2023NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
December 13, 2017NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 1, 2016NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
April 3, 2013NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 7 other inspections on the company page
Other documents for Kaytee Products, Inc.
  • FDA Inspection 1283394 - 2025-09-11
  • FDA Inspection 1224251 - 2023-11-30
  • FDA Inspection 1037298 - 2017-12-13
  • FDA Inspection 985856 - 2016-09-01
  • FDA Inspection 826779 - 2013-04-03

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