FDA Warning Letter — Precision Needle Manufacturing, Inc.

Case 428715 — FEI 3003947796

The FDA took a Warning Letter action against Precision Needle Manufacturing, Inc. on May 25, 2014 (Gyunggi-Do, South Korea). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Precision Needle Manufacturing, Inc.
Date
May 25, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Gyunggi-Do (South Korea)