FDA Inspection 1169144 — Ortek Therapeutics, Inc.

Ortek Therapeutics, Inc. — FEI 3004498471

The FDA completed an inspection of Ortek Therapeutics, Inc. on May 4, 2022 in Roslyn Heights, NY. 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
May 4, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Roslyn Heights, NY (United States)