FDA Inspection 883593 — Multi-Med, Inc.

Multi-Med, Inc. — FEI 1221765

The FDA completed an inspection of Multi-Med, Inc. on June 18, 2014 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
June 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Keene, NH (United States)