FDA Inspection 1289302 — Bios Medical

Bios Medical — FEI 3033273230

The FDA completed an inspection of Bios Medical on Oct 20, 2025 in Nesbit, MS. 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
Oct 20, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Nesbit, MS (United States)

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