# Dujo Logos Inc – FDA Inspection, Jan 4, 2018

Source: https://www.keypedia.com/records/fda_inspections/dujo-logos-inc/f2234739-760d-4e50-9c16-ff1d76a4e739
Source feed: FDA_Inspections

> FDA inspection 1038139 of Dujo Logos Inc, January 04, 2018. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038139
- Company Name: Dujo Logos Inc
- Inspection Date: 2018-01-04
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- FDA Inspection 937609 - 2015-06-24
- FDA Inspection 766353 - 2012-02-06
- FDA Inspection 647582 - 2010-02-22

## Related Officers

- [Company Rep](https://www.keypedia.com/people/joseph-d-gong/c1079a56-5f84-4e0d-9f76-9dc1187e588a)

Company: https://www.keypedia.com/companies/dujo-logos-inc/bfeb301a-d3f5-4eb7-83fd-63537b6ff77f

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