# FDA Inspection 935190 - Dukal Llc - July 13, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/dukal-llc/f7ea1513-7a06-4fb2-9fbf-6acf9cf34e2e/
Source feed: FDA_Inspections

> FDA Inspection 935190 for Dukal Llc on July 13, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935190
- Company Name: Dukal Llc
- Inspection Date: 2015-07-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/dukal-llc/13ba83e4-ad77-4f10-83fd-331a8b9ecd8b

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