# FDA Inspection 785785 - Cylex, Inc. - June 11, 2012

Source: https://www.keypedia.com/records/fda_inspections/cylex-inc/72cb5a67-3c40-4d69-beab-adc0e7a8c535
Source feed: FDA_Inspections

> FDA Inspection 785785 for Cylex, Inc. on June 11, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 785785
- Company Name: Cylex, Inc.
- Inspection Date: 2012-06-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 785785 - 2012-06-11](https://www.keypedia.com/records/fda_inspections/cylex-inc/1f4ce0b9-31e5-415f-a3d9-a25ac6e988fd)
- [FDA Inspection 552589 - 2008-12-17](https://www.keypedia.com/records/fda_inspections/cylex-inc/a4e40955-ab65-469c-a651-ce8b47399166)

Company: https://www.keypedia.com/companies/cylex-inc/8f0272cf-a5ee-45c0-80d7-4a41e455982e

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