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FDA Inspection
•PharmPak, Inc.•March 17, 2017

PharmPak, Inc. – FDA Inspection, Mar 17, 2017

Record Details

This FDA Inspection record concerns PharmPak, Inc., with an inspection on March 17, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
PharmPak, Inc.
Inspection Date
March 17, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • John A. Gonzalez (FDA Associated Person)
View Company Profile

ID · 1e904293-17e9-44f8-ab24-0011047c8da8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1013244
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of PharmPak, Inc.

3
DateClassificationOfficeProject area
December 9, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 18, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for PharmPak, Inc.
  • FDA Inspection 1158404 - 2021-12-09
  • FDA Inspection 782439 - 2012-05-23
  • FDA Inspection 667218 - 2010-06-18

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