# FDA Inspection 1023508 - Persyst Development Corp - 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 for Persyst Development Corp on May 19, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 751467 - 2011-10-27](https://www.keypedia.com/records/fda_inspections/persyst-development-corp/30e25201-16b4-46b2-aad9-e0ec070da380)

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