FDA Warning Letter — Siemens Healthcare Diagnostics, Inc.

Case 285520 — FEI 2517506

The FDA took a Warning Letter action against Siemens Healthcare Diagnostics, Inc. on June 29, 2012 (Newark, DE). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Siemens Healthcare Diagnostics, Inc.
Date
June 29, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Newark, DE (United States)