# I-Tek Medical Inc – FDA Inspection, May 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/51d572dc-6192-49d7-840c-ca108da6af71
Source feed: FDA_Inspections

> FDA inspection 1092862 of I-Tek Medical Inc, May 30, 2019. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092862
- Company Name: I-Tek Medical Inc
- Inspection Date: 2019-05-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 988503 - 2016-09-26
- FDA Inspection 910481 - 2014-11-20
- FDA Inspection 898270 - 2014-09-30

## Related Officers

- [Company Rep](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

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