FDA Inspection 975309 — Gilead Sciences, Inc.

Gilead Sciences, Inc. — FEI 1000523075

The FDA completed an inspection of Gilead Sciences, Inc. on May 11, 2016 in Foster City, 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
May 11, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Foster City, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

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