# FDA Inspection 1008979 - Kalitec Direct, LLC - April 13, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/kalitec-direct-llc/60da3081-39e0-441a-aae1-944e7ad1ad1c
Source feed: FDA_Inspections

> FDA Inspection 1008979 for Kalitec Direct, LLC on April 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008979
- Company Name: Kalitec Direct, LLC
- Inspection Date: 2017-04-13
- 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/kalitec-direct-llc/d5304629-c35e-4bf7-8663-704bf1297334

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