FDA Warning Letter — Activa Brand Products, Inc.

Case 119848 — FEI 1000228839

The FDA took a Warning Letter action against Activa Brand Products, Inc. on Aug 25, 2010 (Cornwall, Canada). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Activa Brand Products, Inc.
Date
Aug 25, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Cornwall (Canada)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.