FDA Inspection 1292016 — Lelypharma BV

Lelypharma BV — FEI 3015660451

The FDA completed an inspection of Lelypharma BV on Sep 26, 2025 in Lelystad. 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
Sep 26, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lelystad (Netherlands)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.