FDA Inspection 1002555 — Mansoor Mirza

Mansoor Mirza — FEI 3012990835

The FDA completed an inspection of Mansoor Mirza on Feb 17, 2017 in Copenhagen O, Capital 2100. 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
Feb 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Copenhagen O, Capital 2100 (Denmark)

Additional Details

Clinical Investigator (CI)

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