FDA Inspection 1294824 — Arne Schwindt, MD

Arne Schwindt, MD — FEI 3039020775

The FDA completed an inspection of Arne Schwindt, MD on Oct 10, 2025 in Hohenzollerning 70. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Oct 10, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Hohenzollerning 70 (Germany)

Additional details

Clinical Investigator (CI)

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