FDA Inspection 1037916 — Estill Medical Technologies, Inc

Estill Medical Technologies, Inc — FEI 3002587972

The FDA completed an inspection of Estill Medical Technologies, Inc on Dec 20, 2017 in Dallas, TX. 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
Dec 20, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)