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FDA Inspection
•AustarPharma, LLC•June 22, 2017

AustarPharma, LLC – FDA Inspection, Jun 22, 2017

Record Details

This FDA Inspection record concerns AustarPharma, LLC, with an inspection on June 22, 2017, issued by the New Jersey District Office, covering human drugs.

Company
AustarPharma, LLC
Inspection Date
June 22, 2017
Product Type
Human Drugs
Office
New Jersey District Office
People
  • Melissa T. Roy (FDA Associated Person)
  • Saleem A. Akhtar
View Company Profile

ID · ff5437cf-d90b-484a-b3f3-d1c17a53201a

Inspection Facts

Inspection number
1015357
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of AustarPharma, LLC

9
DateClassificationOfficeProject area
December 4, 2024VAINew Jersey District OfficePostmarketing Surveillance and Epidemiology: Human Drugs
April 5, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 11, 2019Not classifiedNew Jersey District Office
May 23, 2018VAINew Jersey District OfficeGeneric Drug Evaluation
January 5, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for AustarPharma, LLC
  • FDA Inspection 1236866 - 2024-12-04
  • FDA Inspection 1201798 - 2023-04-05
  • FDA Inspection 1080178 - 2019-02-11
  • FDA Inspection 1052925 - 2018-05-23
  • FDA Inspection 1037881 - 2018-01-05

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