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FDA Inspection
•Teligent Pharma, Inc.•March 8, 2011

Teligent Pharma, Inc. – FDA Inspection, Mar 8, 2011

Record Details

This FDA Inspection record concerns Teligent Pharma, Inc., with an inspection on March 8, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Teligent Pharma, Inc.
Inspection Date
March 8, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 8d2d9dd4-5fd0-4041-adf3-6621db5c67c5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
712964
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.25(a)Training , Education , Experience overall

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Teligent Pharma, Inc.

8
DateClassificationOfficeProject area
August 31, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 20, 2019Not classifiedNew Jersey District OfficeDrug Quality Assurance
October 19, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2016NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
December 19, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Teligent Pharma, Inc.
  • FDA Inspection 1150271 - 2021-08-31
  • FDA Inspection 1090090 - 2019-05-20
  • FDA Inspection 1032023 - 2017-10-19
  • FDA Inspection 956413 - 2016-01-22
  • FDA Inspection 859472 - 2013-12-19

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