FDA Inspection 1076127 — Lyndon Jones, PhD

Lyndon Jones, PhD — FEI 3014753579

The FDA completed an inspection of Lyndon Jones, PhD on Dec 6, 2018 in Waterloo. 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
Dec 6, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Waterloo (Canada)

Additional Details

Clinical Investigator (CI)

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