FDA Inspection 831933 — Neutraderm, Inc.

Neutraderm, Inc. — FEI 3006402197

The FDA completed an inspection of Neutraderm, Inc. on Apr 26, 2013 in Chatsworth, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chatsworth, CA (United States)