FDA Inspection 1116058 — Melinda Nye PHD

Melinda Nye PHD — FEI 3015880970

The FDA completed an inspection of Melinda Nye PHD on Jan 16, 2020 in Burlington, 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
Jan 16, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Burlington, NC (United States)

Additional details

Clinical Investigator (CI)

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