FDA Warning Letter — ThyssenKrupp Access Manufacturing, LLC

Case 271496 — FEI 1000139742

The FDA took a Warning Letter action against ThyssenKrupp Access Manufacturing, LLC on March 27, 2012 (Roanoke, IL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
ThyssenKrupp Access Manufacturing, LLC
Date
March 27, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Roanoke, IL (United States)