# FDA Inspection 898270 - I-Tek Medical Inc - September 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/7ef45ee5-e050-4f91-a916-be65606efbd8
Source feed: FDA_Inspections

> FDA Inspection 898270 for I-Tek Medical Inc on September 30, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 898270
- Company Name: I-Tek Medical Inc
- Inspection Date: 2014-09-30
- 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/i-tek-medical-inc/8b142073-cb0b-466c-b118-9388866f4812

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