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FDA Inspection 1278307 — Adroit Medical Systems Inc

Adroit Medical Systems Inc — FEI 1000111140

The FDA completed an inspection of Adroit Medical Systems Inc on July 11, 2025 in Loudon, TN. 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
July 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Loudon, TN (United States)

Facility

Other inspections at this facility

  • 1085944 (NAI Thu Apr 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1017646 (VAI Wed Jul 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 765950 (VAI Mon Jan 23 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 642668 (NAI Thu Jan 28 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources