FDA Warning Letter — 9mm Special Effects

Case 443368 — FEI 3009537647

The FDA took a Warning Letter action against 9mm Special Effects on May 19, 2015 (Haiku, HI). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
9mm Special Effects
Date
May 19, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Haiku, HI (United States)