FDA Inspection 1257901 — Norfolk Medical Products, Inc.

Norfolk Medical Products, Inc. — FEI 1450392

The FDA completed an inspection of Norfolk Medical Products, Inc. on Dec 18, 2024 in Skokie, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 18, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Skokie, IL (United States)