FDA Inspection 807743 — Annex Medical, Inc.

Annex Medical, Inc. — FEI 2183873

The FDA completed an inspection of Annex Medical, Inc. on November 5, 2012 in Minnetonka, 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
November 5, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)