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FDA Inspection
•Qilu SYNVA Pharmaceutical Co. Ltd•July 26, 2019

Qilu SYNVA Pharmaceutical Co. Ltd – FDA Inspection, Jul 26, 2019

Record Details

This FDA Inspection record concerns Qilu SYNVA Pharmaceutical Co. Ltd, with an inspection on July 26, 2019, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Qilu SYNVA Pharmaceutical Co. Ltd
Inspection Date
July 26, 2019
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Cheryl A. Clausen
View Company Profile

ID · a2d93be4-63c0-40b0-a088-b95799038fdb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1098879
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

Other FDA inspections of Qilu SYNVA Pharmaceutical Co. Ltd

3
DateClassificationOfficeProject area
May 16, 2025Not classifiedOffice of Inspections and Investigations
December 13, 2019NAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
June 17, 2016NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Qilu SYNVA Pharmaceutical Co. Ltd
  • FDA Inspection 1275186 - 2025-05-16
  • FDA Inspection 1115250 - 2019-12-13
  • FDA Inspection 980987 - 2016-06-17

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