FDA Inspection 1078705 — Hendrik-Tobias Arkenau

Hendrik-Tobias Arkenau — FEI 3013203956

The FDA completed an inspection of Hendrik-Tobias Arkenau on Jan 10, 2019 in London. 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
Jan 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
London (United Kingdom)

Additional Details

Clinical Investigator (CI)

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