FDA Inspection
Perry Dynamics IncPerry Dynamics Inc – FDA Inspection, Aug 19, 2016
Record Details
This FDA Inspection record concerns Perry Dynamics Inc, with an inspection on August 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perry Dynamics Inc
- Inspection Date
- August 19, 2016
- Product Type
- Devices
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ID · 3431f89a-5700-4173-b8a9-c646d8d3c209
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 984888
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.30(j)Design history file
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Perry Dynamics Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 20, 2026 | NAI | 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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