FDA Warning Letter — Customed, Inc.

Case 74243 — FEI 2648727

The FDA took a Warning Letter action against Customed, Inc. on Sep 11, 2009 (Fajardo, PR). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Customed, Inc.
Date
Sep 11, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Fajardo, PR (United States)

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