FDA Inspection 1039581 — Michael Van Der Linden

Michael Van Der Linden — FEI 3013833845

The FDA completed an inspection of Michael Van Der Linden on Jan 19, 2018 in Durban. 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 19, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Durban (South Africa)

Additional Details

Clinical Investigator (CI)

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