FDA Inspection 1032023 — Teligent Pharma, Inc.

Teligent Pharma, Inc. — FEI 1000526875

The FDA completed an inspection of Teligent Pharma, Inc. on Oct 19, 2017 in Buena, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 19, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Buena, NJ (United States)

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