FDA Inspection 745531 — Perma Pure LLC

Perma Pure LLC — FEI 2244684

The FDA completed an inspection of Perma Pure LLC on September 19, 2011 in Lakewood, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 19, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Lakewood, NJ (United States)

Citations

IDCFRDescription
310821 CFR 820.70(e)Contamination control, Lack of or inadequate procedures