FDA Inspection 1278307 — Adroit Medical Systems Inc

Adroit Medical Systems Inc — FEI 1000111140

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.