FDA Inspection 1038972 — Kathryn Menard

Kathryn Menard — FEI 3013924614

The FDA completed an inspection of Kathryn Menard on Jan 9, 2018 in Chapel Hill, 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 9, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chapel Hill, NC (United States)

Additional Details

Clinical Investigator (CI)

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