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FDA Inspection 1046904 — Linda Morrow, MD

Linda Morrow, MD — FEI 3014140948

The FDA completed an inspection of Linda Morrow, MD on Mar 7, 2018 in Chula Vista, CA. 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
Mar 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chula Vista, CA (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

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