FDA Warning Letter — Piezosurgery Inc

Case 113710 — FEI 3005282635

The FDA took a Warning Letter action against Piezosurgery Inc on June 8, 2010 (Hilliard, OH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Piezosurgery Inc
Date
June 8, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Hilliard, OH (United States)