FDA Warning Letter — PerioSeal, Inc.

Case 374239 — FEI 3005124408

The FDA took a Warning Letter action against PerioSeal, Inc. on October 29, 2012 (Little Rock, AR). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
PerioSeal, Inc.
Date
October 29, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Little Rock, AR (United States)