FDA Inspection 785066 — Sterilmed Inc.

Sterilmed Inc. — FEI 3001237663

The FDA completed an inspection of Sterilmed Inc. on May 31, 2012 in Maple Grove, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 31, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Maple Grove, MN (United States)