FDA Warning Letter — Peter Schiff Enterprises

Case 406601 — FEI 1000112898

The FDA took a Warning Letter action against Peter Schiff Enterprises on July 31, 2013 (Cookeville, TN). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Peter Schiff Enterprises
Date
July 31, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Cookeville, TN (United States)