# Perry Dynamics Inc – FDA 483, May 20, 2026

Source: https://www.keypedia.com/records/483/perry-dynamics-inc/503e6448-b3fb-458a-bd48-9348506f1397

> FDA 483 for Perry Dynamics Inc on May 20, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Perry Dynamics Inc
- Inspection Date: 2026-05-20
- Product Type: device
- Office Name: Chicago District Office
- Summary: Perry Dynamics Inc. in Decatur, IL, was inspected regarding its medical device manufacturing, specifically for its Class II Isokinetic Testing and Evaluation Systems. The inspection revealed significant deficiencies in the firm's risk management processes, UDI labeling for its devices, and the submission of required device information to the GUDID. These observations indicate a failure to comply with critical regulatory requirements for medical device quality and traceability.

## Related Officers

- [Clifford F. Long](https://www.keypedia.com/people/clifford-f-long/846e5a0c-cb7c-421c-86aa-be9fddfbaaba)

Company: https://www.keypedia.com/companies/perry-dynamics-inc/610ea839-af16-4511-b8b3-4082523dc0b8

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669