FDA Inspection 931750 — IQVIA

IQVIA — FEI 1000111052

The FDA completed an inspection of IQVIA on Jun 19, 2015 in Durham, NC. 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
Jun 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Durham, NC (United States)

Additional details

Sponsor, Contract Research Organization

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