FDA Inspection 1266115 — Synthekine Inc.

Synthekine Inc. — FEI 3015505672

The FDA completed an inspection of Synthekine Inc. on April 2, 2025 in Menlo Park, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 2, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Menlo Park, CA (United States)

Additional Details

Sponsor, Contract Research Organization