FDA Warning Letter — Spryson America Inc.

Case 410822 — FEI 2519945

The FDA took a Warning Letter action against Spryson America Inc. on September 11, 2013 (Pittsburgh, PA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Spryson America Inc.
Date
September 11, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Pittsburgh, PA (United States)