FDA Inspection 1320618 — Ablynx NV

Ablynx NV — FEI 3008915297

The FDA completed an inspection of Ablynx NV on May 24, 2024 in Gent. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gent (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)