FDA Inspection 855040 — CRI - Maple Grove

CRI - Maple Grove — FEI 3010133999

The FDA completed an inspection of CRI - Maple Grove on Nov 14, 2013 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
Nov 14, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)