# FDA Inspection 906062 - CD Leycom - November 06, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/cd-leycom/e214a422-c8e3-4d35-b156-4a35d4bdcf25
Source feed: FDA_Inspections

> FDA Inspection 906062 for CD Leycom on November 06, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 906062
- Company Name: CD Leycom
- Inspection Date: 2014-11-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 653947 - 2010-03-04](https://www.globalkeysolutions.net/records/fda_inspections/cd-leycom/f98e4094-a3b9-4190-b05c-b9b1131bae15)

Company: https://www.globalkeysolutions.net/companies/cd-leycom/05021437-5cf1-4158-8b0a-2ec7e22710fc

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