FDA Inspection 545897 — UMA, Inc.

UMA, Inc. — FEI 2412254

The FDA completed an inspection of UMA, Inc. on November 10, 2008 in Dayton, VA. 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 10, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Dayton, VA (United States)