# FDA Inspection 1060965 - Sciteck Diagnostics - August 03, 2018

Source: https://www.keypedia.com/records/fda_inspections/sciteck-diagnostics/cfb96b39-37c8-4167-adc4-7b9d62fdc54e
Source feed: FDA_Inspections

> FDA Inspection 1060965 for Sciteck Diagnostics on August 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060965
- Company Name: Sciteck Diagnostics
- Inspection Date: 2018-08-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060965 - 2018-08-03](https://www.keypedia.com/records/fda_inspections/sciteck-diagnostics/a41eb75e-b2ef-474c-8d7c-90808cf68d05)

Company: https://www.keypedia.com/companies/sciteck-diagnostics/3b8343d1-fac8-427e-a095-e9f55f79b292

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