FDA Inspection 934536 — Theravance Biopharma US, Inc.

Theravance Biopharma US, Inc. — FEI 3006131466

The FDA completed an inspection of Theravance Biopharma US, Inc. on Jun 26, 2015 in South San Francisco, CA. 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
Jun 26, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
South San Francisco, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)