# Sciteck Diagnostics – FDA Inspection, Aug 3, 2018

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

> FDA inspection 1060965 of Sciteck Diagnostics, August 03, 2018. Classification: No Action Indicated (NAI). 7 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 1320280 - 2026-06-03](https://www.keypedia.com/records/fda_inspections/sciteck-diagnostics/818bb091-4048-4383-bd88-68403e3ad2a3)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

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