FDA Inspection 561296 — Bestvite, Inc.

Bestvite, Inc. — FEI 3007190452

The FDA completed an inspection of Bestvite, Inc. on Feb 2, 2009 in Sun Valley, 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
Feb 2, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Sun Valley, CA (United States)

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