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FDA Inspection
•Lannett Company, Inc.•August 17, 2012

Lannett Company, Inc. – FDA Inspection, Aug 17, 2012

Record Details

This FDA Inspection record concerns Lannett Company, Inc., with an inspection on August 17, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Lannett Company, Inc.
Inspection Date
August 17, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 4d8a60f7-a67b-4a18-ba39-ad1342f5bf2f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
803870
FDA center
Human Drugs
Project area
Bioresearch Monitoring

Other FDA inspections of Lannett Company, Inc.

9
DateClassificationOfficeProject area
March 25, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 25, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2017NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
September 16, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 6, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Lannett Company, Inc.
  • FDA Inspection 1167830 - 2022-03-25
  • FDA Inspection 1081137 - 2019-01-25
  • FDA Inspection 1018610 - 2017-06-22
  • FDA Inspection 987590 - 2016-09-16
  • FDA Inspection 844132 - 2013-08-06

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