FDA Inspection 666748 — Multi-Med, Inc.

Multi-Med, Inc. — FEI 1221765

The FDA completed an inspection of Multi-Med, Inc. on April 30, 2010 in Keene, NH. 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
April 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Keene, NH (United States)