FDA Warning Letter — Barton-Carey Medical Products Inc

Case 360239 — FEI 1527179

The FDA took a Warning Letter action against Barton-Carey Medical Products Inc on Dec 10, 2012 (Maumee, OH). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
Barton-Carey Medical Products Inc
Date
Dec 10, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Maumee, OH (United States)

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