FDA Warning Letter — Teligent Pharma, Inc.

Case 587592 — FEI 1000526875

The FDA took a Warning Letter action against Teligent Pharma, Inc. on Nov 26, 2019 (Buena, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Teligent Pharma, Inc.
Date
Nov 26, 2019
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Buena, NJ (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.