FDA Inspection
Perry Dynamics IncPerry Dynamics Inc – FDA Inspection, May 20, 2026
Record Details
This FDA Inspection record concerns Perry Dynamics Inc, with an inspection on May 20, 2026, issued by the Center for Devices and Radiological Health, covering medical devices & rad health.
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ID · ec17e281-c4fb-4d9e-85eb-10af06fde361
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1318306
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- ISO 13485:2016 Clause 4.1.2Risk-based approach not applied to QMS processes
- 21 CFR 830Devices subject to device identification GUDID data submission requirements.
- 21 CFR 801.20(a)Label to bear a unique device identifier
- 21 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
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Other FDA inspections of Perry Dynamics Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 19, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 19, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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