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FDA Inspection
•Radiation Products Design,Inc•March 4, 2026

Radiation Products Design,Inc – FDA Inspection, Mar 4, 2026

Record Details

This FDA Inspection record concerns Radiation Products Design,Inc, with an inspection on March 4, 2026, issued by the Minneapolis District Office, covering medical devices & rad health.

Company
Radiation Products Design,Inc
Inspection Date
March 4, 2026
Product Type
Medical Devices & Rad Health
Office
Minneapolis District Office
Person
  • Christina L. Bigham (FDA Associated Person)
View Company Profile

ID · 3d1b629b-9af0-4c66-a818-c0ef2ad0090f

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1306546
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. ISO 13485:2016 Clause 7.1Product realization risk management processes not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Radiation Products Design,Inc

3
DateClassificationOfficeProject area
April 10, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 6, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
March 19, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Radiation Products Design,Inc
  • FDA Inspection 1049026 - 2018-04-10
  • FDA Inspection 807050 - 2012-11-06
  • FDA Inspection 653205 - 2010-03-19

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