FDA Inspection 1109177 — GVS TM, Inc

GVS TM, Inc — FEI 2013342

The FDA completed an inspection of GVS TM, Inc on Sep 25, 2019 in Covina, 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
Sep 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Covina, CA (United States)

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