FDA Inspection 1029655 — Kristin N. Castorino, D.O.

Kristin N. Castorino, D.O. — FEI 3013709310

The FDA completed an inspection of Kristin N. Castorino, D.O. on Sep 28, 2017 in Santa Barbara, 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
Sep 28, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Barbara, CA (United States)

Additional details

Clinical Investigator (CI)

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