FDA Inspection 734394 — Intercharm, Inc.

Intercharm, Inc. — FEI 3008810227

The FDA completed an inspection of Intercharm, Inc. on Aug 10, 2011 in Hallandale Beach, FL. 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
Aug 10, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Hallandale Beach, FL (United States)