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FDA Inspection
•King Bio Inc.•July 20, 2018

King Bio Inc. – FDA Inspection, Jul 20, 2018

Record Details

This FDA Inspection record concerns King Bio Inc., with an inspection on July 20, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
King Bio Inc.
Inspection Date
July 20, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Melanie M. Walker
  • Rachael L. Derby (Issuing Officer)
  • Sonya M. Edmonds (FDA Associated Person)
View Company Profile

ID · db39b8b3-2074-480f-ba35-fa6fc5a72646

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1059419
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued
Enforcement
Warning Letter

Other FDA inspections of King Bio Inc.

7
DateClassificationOfficeProject area
July 28, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 12, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 2, 2017VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 4, 2015VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 15, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for King Bio Inc.
  • FDA Inspection 1215129 - 2023-07-28
  • FDA Inspection 1149278 - 2021-08-12
  • FDA Inspection 1004463 - 2017-03-02
  • FDA Inspection 941497 - 2015-09-04
  • FDA Inspection 900797 - 2014-10-15

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Contact
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