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FDA Inspection 1035093 — Lauralyn A McIntyre, MD

Lauralyn A McIntyre, MD — FEI 3013872375

The FDA completed an inspection of Lauralyn A McIntyre, MD on Nov 9, 2017 in Ottawa. 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
Nov 9, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Ottawa (Canada)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

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