# Persyst Development Corp – FDA Inspection, May 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/persyst-development-corp/615fefac-e5a8-484e-a1c9-e9dbadd1c096
Source feed: FDA_Inspections

> FDA inspection 1023508 of Persyst Development Corp, May 19, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023508
- Company Name: Persyst Development Corp
- Inspection Date: 2017-05-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1082695 - 2018-04-03](https://www.keypedia.com/records/fda_inspections/persyst-development-corp/ada13fde-03ae-4806-a212-b6f46ac9bd30)
- FDA Inspection 751467 - 2011-10-27

## Related Officers

- [Company Rep](https://www.keypedia.com/people/charles-l-larson/4232255d-bfd6-4616-a854-c801e4c23e1c)

Company: https://www.keypedia.com/companies/persyst-development-corp/ebd5f381-b914-4ff8-b8b0-a8a803764b34

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7