FDA Inspection 555083 — Onyx Medical, LLC

Onyx Medical, LLC — FEI 1043653

The FDA completed an inspection of Onyx Medical, LLC on December 30, 2008 in Bartlett, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 30, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)