Home / Inspections / 822737

FDA Inspection 822737 — Symbios Medical Products, LLC

Symbios Medical Products, LLC — FEI 3005203102

The FDA completed an inspection of Symbios Medical Products, LLC on March 19, 2013 in Indianapolis, IN. 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
March 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Indianapolis, IN (United States)

Facility

Other inspections at this facility

  • 834119 (OAI Mon Jun 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 722543 (VAI Fri Apr 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 604393 (VAI Wed Aug 26 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources