FDA Warning Letter — Pinook USA, LLC

Case 292797 — FEI 3008113239

The FDA took a Warning Letter action against Pinook USA, LLC on June 14, 2012 (Orlando, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Pinook USA, LLC
Date
June 14, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Orlando, FL (United States)