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FDA Inspection
•Dongying Tiandong Pharmaceutical Co Ltd•October 19, 2018

Dongying Tiandong Pharmaceutical Co Ltd – FDA Inspection, Oct 19, 2018

Record Details

This FDA Inspection record concerns Dongying Tiandong Pharmaceutical Co Ltd, with an inspection on October 19, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Dongying Tiandong Pharmaceutical Co Ltd
Inspection Date
October 19, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Marijo B. Kambere
View Company Profile

ID · d4f21e18-8c07-4334-95b4-beab07854cad

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1071826
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Dongying Tiandong Pharmaceutical Co Ltd

2
DateClassificationOfficeProject area
October 16, 2015OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 2, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Dongying Tiandong Pharmaceutical Co Ltd
  • FDA Inspection 953580 - 2015-10-16
  • FDA Inspection 844016 - 2013-08-02

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