FDA Warning Letter — Perma Pure LLC

Case 133030 — FEI 2244684

The FDA took a Warning Letter action against Perma Pure LLC on September 21, 2010 (Lakewood, NJ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Perma Pure LLC
Date
September 21, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Lakewood, NJ (United States)