# FDA Inspection 1026761 - Candelis Inc - September 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/candelis-inc/0949f4e4-2f27-42bb-b6d7-0352c8fa66b0
Source feed: FDA_Inspections

> FDA Inspection 1026761 for Candelis Inc on September 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026761
- Company Name: Candelis Inc
- Inspection Date: 2017-09-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026761 - 2017-09-01](https://www.keypedia.com/records/fda_inspections/candelis-inc/cc3cdc88-9973-4945-8739-fd619addbc20)

Company: https://www.keypedia.com/companies/candelis-inc/30b4c45d-9590-4d87-b61c-c54d0cd0e962

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