FDA Inspection
Dr. Joel Kaplan Inc.Dr. Joel Kaplan Inc. – FDA Inspection, Jul 17, 2013
Record Details
This FDA Inspection record concerns Dr. Joel Kaplan Inc., with an inspection on July 17, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Dr. Joel Kaplan Inc.
- Inspection Date
- July 17, 2013
- Product Type
- Devices
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ID · 7e01a97d-cbdf-4e29-83c1-1022ae975c00
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 838587
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Dr. Joel Kaplan Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 27, 2025 | Not classified | Los Angeles District Office | |
| June 30, 2023 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 16, 2021 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| November 1, 2017 | VAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| December 18, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Dr. Joel Kaplan Inc.
- FDA Inspection 1277023 - 2025-06-27
- FDA Inspection 1209291 - 2023-06-30
- FDA Inspection 1159322 - 2021-12-16
- FDA Inspection 1030651 - 2017-11-01
- FDA Inspection 907606 - 2014-12-18
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