FDA Inspection 1246471 — CTK Biotech, Inc.

CTK Biotech, Inc. — FEI 3003952975

The FDA completed an inspection of CTK Biotech, Inc. on Aug 8, 2024 in Poway, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 8, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Poway, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures