FDA Inspection 728373 — DMS Holdings, Inc.

DMS Holdings, Inc. — FEI 1000143485

The FDA completed an inspection of DMS Holdings, Inc. on June 7, 2011 in Waukegan, IL. 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
June 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Waukegan, IL (United States)