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FDA Inspection
•Retorte GmbH Selenium Chemicals & Metals•September 15, 2017

Retorte GmbH Selenium Chemicals & Metals – FDA Inspection, Sep 15, 2017

Record Details

This FDA Inspection record concerns Retorte GmbH Selenium Chemicals & Metals, with an inspection on September 15, 2017, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Retorte GmbH Selenium Chemicals & Metals
Inspection Date
September 15, 2017
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Samantha J. Bradley (FDA Associated Person)
View Company Profile

ID · f7c611e2-0916-4151-bc9a-f13686b61290

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1029318
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

Other FDA inspections of Retorte GmbH Selenium Chemicals & Metals

3
DateClassificationOfficeProject area
November 16, 2023VAIMonitoring of Marketed Animal Drugs, Feed, and Devices
July 23, 2015NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
July 15, 2011NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Retorte GmbH Selenium Chemicals & Metals
  • FDA Inspection 1305810 - 2023-11-16
  • FDA Inspection 939286 - 2015-07-23
  • FDA Inspection 739380 - 2011-07-15

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