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FDA Inspection
•Jeron Electronic Systems Inc.•October 7, 2026

Jeron Electronic Systems Inc. – FDA Inspection, Oct 7, 2026

Record Details

This FDA Inspection record concerns Jeron Electronic Systems Inc., with an inspection on October 7, 2026, issued by the Center for Devices and Radiological Health, covering devices.

Company
Jeron Electronic Systems Inc.
Inspection Date
October 7, 2026
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fbe4192f-191d-4860-a303-207f265e2c75

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1342246
Project area
Postmarket Assurance: Devices

FDA Citations

2
  1. ISO 13485:2016 Clause 7.1Product realization risk management processes not documented
  2. ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Jeron Electronic Systems Inc.

2
DateClassificationOfficeProject area
December 4, 2024NAIChicago District OfficePostmarket Assurance: Medical Devices
June 20, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Jeron Electronic Systems Inc.
  • FDA Inspection 1255817 - 2024-12-04
  • FDA Inspection 1093944 - 2019-06-20

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