# Surgitech Inc – FDA Inspection, Aug 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/surgitech-inc/c6eb683b-f42d-40b7-80a9-e9f213f27879
Source feed: FDA_Inspections

> FDA inspection 1023579 of Surgitech Inc, August 23, 2017. Classification: No Action Indicated (NAI). 3 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: 1023579
- Company Name: Surgitech Inc
- Inspection Date: 2017-08-23
- 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: 3

## Related Documents

- [FDA Inspection 1214483 - 2023-08-10](https://www.keypedia.com/records/fda_inspections/surgitech-inc/c90b0e59-a59a-490a-b250-80f76797d701)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

Company: https://www.keypedia.com/companies/surgitech-inc/2272bfc6-a009-4b35-bdac-84f8c10cb783

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