FDA Inspection 915250 — DermaRite Industries, LLC

DermaRite Industries, LLC — FEI 1000526900

The FDA completed an inspection of DermaRite Industries, LLC on Feb 23, 2015 in North Bergen, NJ. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 23, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
North Bergen, NJ (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
183321 CFR 211.84(d)(1)Identity Testing of Each Component

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