FDA Inspection 1229145 — Multi-Med, Inc.

Multi-Med, Inc. — FEI 1221765

The FDA completed an inspection of Multi-Med, Inc. on September 19, 2024 in Keene, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Keene, NH (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
323521 CFR 820.72(a)Equipment control activity documentation
331321 CFR 820.120(d)Records, DHR {see also 820.184(e)}