FDA Inspection 652014 — Grove Corp.

Grove Corp. — FEI 1928347

The FDA completed an inspection of Grove Corp. on Mar 16, 2010 in Carefree, AZ. 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
Mar 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Carefree, AZ (United States)