FDA Warning Letter — Greiner Bio-One North America, Inc.

Case 606266 — FEI 3001451379

The FDA took a Warning Letter action against Greiner Bio-One North America, Inc. on April 16, 2020 (Monroe, NC). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Greiner Bio-One North America, Inc.
Date
April 16, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Monroe, NC (United States)