# Cyberlogic, Inc. – FDA Inspection, Mar 25, 2019

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

> FDA inspection 1083804 of Cyberlogic, Inc., March 25, 2019. Classification: No Action Indicated (NAI). 8 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

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## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/colin-e-tack/5bdbf977-d4ac-48fe-81cc-ada89379ed0d)
- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)
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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