FDA Inspection 631022 — Grand Medical

Grand Medical — FEI 3004873266

The FDA completed an inspection of Grand Medical on November 20, 2009 in Kansas City, MO. 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 20, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kansas City, MO (United States)