FDA Inspection 644583 — Axiobionics, LLC

Axiobionics, LLC — FEI 3008525454

The FDA completed an inspection of Axiobionics, LLC on Feb 8, 2010 in Ann Arbor, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 8, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Ann Arbor, MI (United States)

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