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FDA Inspection
•G Production, Inc.•December 8, 2017

G Production, Inc. – FDA Inspection, Dec 8, 2017

Record Details

This FDA Inspection record concerns G Production, Inc., with an inspection on December 8, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
G Production, Inc.
Inspection Date
December 8, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Deyaa Shaheen (FDA Associated Person)
View Company Profile

ID · 901acd1b-8a50-4b49-a72d-fb3b165620b7

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1034500
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls

Full citation text and observation details available on the Dashboard.

Other FDA inspections of G Production, Inc.

5
DateClassificationOfficeProject area
February 17, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 13, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 29, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 4, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for G Production, Inc.
  • FDA Inspection 1199218 - 2023-02-17
  • FDA Inspection 917458 - 2015-02-13
  • FDA Inspection 834222 - 2013-05-17
  • FDA Inspection 750113 - 2011-09-29
  • FDA Inspection 613134 - 2009-09-04

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