FDA Inspection 795363 — Theravance Biopharma US, Inc.

Theravance Biopharma US, Inc. — FEI 3006131466

The FDA completed an inspection of Theravance Biopharma US, Inc. on Aug 27, 2012 in South San Francisco, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 27, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
South San Francisco, CA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)