# FDA Inspection 563983 - Kiltex Corporation - February 05, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/kiltex-corporation/6f83bc9a-1bcb-4fda-914d-f55619232df7
Source feed: FDA_Inspections

> FDA Inspection 563983 for Kiltex Corporation on February 05, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 563983
- Company Name: Kiltex Corporation
- Inspection Date: 2009-02-05
- 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/kiltex-corporation/a1fb0c1e-b682-403b-a339-7607966a4284

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