FDA Inspection 1277023 — Dr. Joel Kaplan, Inc.

Dr. Joel Kaplan, Inc. — FEI 3001890611

The FDA completed an inspection of Dr. Joel Kaplan, Inc. on Jun 27, 2025 in San Diego, 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
Jun 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

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