# FDA Inspection 988503 - I-Tek Medical Inc - September 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/4a9b5024-c540-439f-a3ff-d3f0b86d6676
Source feed: FDA_Inspections

> FDA Inspection 988503 for I-Tek Medical Inc on September 26, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 988503
- Company Name: I-Tek Medical Inc
- Inspection Date: 2016-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1092862 - 2019-05-30](https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/2bb0c668-8bc8-4cf5-bc0e-7aeb8fbf5b47)
- [FDA Inspection 1092862 - 2019-05-30](https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/2f9e8169-d03c-471a-857d-294ba9464fe1)
- [FDA Inspection 1092862 - 2019-05-30](https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/51d572dc-6192-49d7-840c-ca108da6af71)
- [FDA Inspection 910481 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/10e68c32-70b0-42e0-82b5-7ce4973b1e50)
- [FDA Inspection 898270 - 2014-09-30](https://www.keypedia.com/records/fda_inspections/i-tek-medical-inc/7ef45ee5-e050-4f91-a916-be65606efbd8)

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