FDA Warning Letter — Primus Corporation

Case 607698 — FEI 1931251

The FDA took a Warning Letter action against Primus Corporation on August 12, 2020 (Kansas City, MO). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Primus Corporation
Date
August 12, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Kansas City, MO (United States)