FDA Inspection 1072292 — Odyssey Medical Technologies, LLC.

Odyssey Medical Technologies, LLC. — FEI 3000205819

The FDA completed an inspection of Odyssey Medical Technologies, LLC. on August 8, 2018 in Bartlett, 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
August 8, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)