Home / Inspections / 768808

FDA Inspection 768808 — Onyx Medical, LLC

Onyx Medical, LLC — FEI 1043653

The FDA completed an inspection of Onyx Medical, LLC on February 13, 2012 in Bartlett, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)

Facility

Other inspections at this facility

  • 1303054 (VAI Fri Feb 13 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1169394 (NAI Thu Apr 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1015584 (NAI Fri Jun 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 555083 (NAI Tue Dec 30 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources