FDA Warning Letter — Advanced Interventional Pain Ctr IRB

Case 416383 — FEI 3010275991

The FDA took a Warning Letter action against Advanced Interventional Pain Ctr IRB on Feb 7, 2014 (Lafayette, IN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Advanced Interventional Pain Ctr IRB
Date
Feb 7, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Lafayette, IN (United States)

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