FDA Inspection 1032023 — Teligent Pharma, Inc.

Teligent Pharma, Inc. — FEI 1000526875

The FDA completed an inspection of Teligent Pharma, Inc. on October 19, 2017 in Buena, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

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