FDA Warning Letter — Axiobionics, LLC

Case 353558 — FEI 3008525454

The FDA took a Warning Letter action against Axiobionics, LLC on Dec 7, 2012 (Ann Arbor, MI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Axiobionics, LLC
Date
Dec 7, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Ann Arbor, MI (United States)

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