# FDA Inspection 1038139 - Dujo Logos Inc - January 04, 2018

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

> FDA Inspection 1038139 for Dujo Logos Inc on January 04, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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