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FDA Inspection 1201082 — Daily Medical Products, Inc.

Daily Medical Products, Inc. — FEI 2083299

The FDA completed an inspection of Daily Medical Products, Inc. on March 21, 2023 in Plymouth, MN. 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
March 21, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plymouth, MN (United States)

Facility

Other inspections at this facility

  • 1016104 (NAI Thu Apr 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 853083 (NAI Tue Oct 29 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 724943 (VAI Thu May 05 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources