FDA Inspection 1054584 — Tytek Medical Inc

Tytek Medical Inc — FEI 3004551550

The FDA completed an inspection of Tytek Medical Inc on April 23, 2018 in West Chester, OH. 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
April 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, OH (United States)