FDA Warning Letter — Peter Schiff Enterprises

Case 727888 — FEI 1000112898

The FDA took a Warning Letter action against Peter Schiff Enterprises on Aug 26, 2026 (Cookeville, TN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Peter Schiff Enterprises
Date
Aug 26, 2026
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Cookeville, TN (United States)