FDA Inspection 1251480 — Rechon Life Science AB

Rechon Life Science AB — FEI 3002806978

The FDA completed an inspection of Rechon Life Science AB on Sep 6, 2024 in Limhamn. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Sep 6, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Limhamn (Sweden)

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