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FDA Inspection 1277023 — Dr. Joel Kaplan, Inc.

Dr. Joel Kaplan, Inc. — FEI 3001890611

The FDA completed an inspection of Dr. Joel Kaplan, Inc. on June 27, 2025 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1209291 (OAI Fri Jun 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1159322 (NAI Thu Dec 16 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1030651 (VAI Wed Nov 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 907606 (VAI Thu Dec 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 838587 (OAI Wed Jul 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources