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FDA Inspection
•Patheon API Manufacturing Inc•March 30, 2018

FDA Inspection 1052718 - Patheon API Manufacturing Inc - March 30, 2018

Record Details

This FDA Inspection record concerns Patheon API Manufacturing Inc, with an inspection on March 30, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Patheon API Manufacturing Inc
Inspection Date
March 30, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 16a4ac0c-ec73-4a70-b34e-62284b7044d4

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1052718
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Patheon API Manufacturing Inc

2
DateClassificationOfficeProject area
November 26, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 30, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Patheon API Manufacturing Inc
  • FDA Inspection 907324 - 2014-11-26
  • FDA Inspection 717250 - 2011-03-30

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