FDA Warning Letter — E.A. Beck & Co.

Case 132031 — FEI 2080222

The FDA took a Warning Letter action against E.A. Beck & Co. on December 14, 2010 (Schaumburg, IL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
E.A. Beck & Co.
Date
December 14, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Schaumburg, IL (United States)