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FDA Inspection 656148 — Anulex Technologies Inc

Anulex Technologies Inc — FEI 3005501497

The FDA completed an inspection of Anulex Technologies Inc on April 8, 2010 in Eden Prairie, MN. 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
April 8, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)

Facility

Other inspections at this facility

  • 835254 (NAI Mon May 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 680312 (OAI Wed Sep 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources