FDA Inspection 1248255 — Syrinx Bioanalytics Oy

Syrinx Bioanalytics Oy — FEI 3010952795

The FDA completed an inspection of Syrinx Bioanalytics Oy on Aug 9, 2024 in Turku. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 9, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Turku (Finland)

Additional Details

Bioanalytical BA/BE