# FDA Inspection 1083804 - Cyberlogic, Inc. - March 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/cyberlogic-inc/f5947025-fb4f-43a2-95b0-54da02e4f664
Source feed: FDA_Inspections

> FDA Inspection 1083804 for Cyberlogic, Inc. on March 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1083804
- Company Name: Cyberlogic, Inc.
- Inspection Date: 2019-03-25
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1214732 - 2023-05-24](https://www.keypedia.com/records/fda_inspections/cyberlogic-inc/53cb1d82-c8f9-40f3-9858-b4053111377f)
- [FDA Inspection 1083804 - 2019-03-25](https://www.keypedia.com/records/fda_inspections/cyberlogic-inc/b12215c1-4079-4cd9-93e1-e581f43786b4)

Company: https://www.keypedia.com/companies/cyberlogic-inc/8c92436b-d635-476b-8233-cd4ea7b57db6

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