# FDA Inspection 1029049 - Vortek Surgical, LLC - September 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/vortek-surgical-llc/e55b4821-06c9-4c2f-9f1e-e0ed745d7bf1
Source feed: FDA_Inspections

> FDA Inspection 1029049 for Vortek Surgical, LLC on September 27, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029049
- Company Name: Vortek Surgical, LLC
- Inspection Date: 2017-09-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029049 - 2017-09-27](https://www.keypedia.com/records/fda_inspections/vortek-surgical-llc/b689d296-88bc-441e-b974-d970f77dd7c4)
- [FDA Inspection 883476 - 2014-06-18](https://www.keypedia.com/records/fda_inspections/vortek-surgical-llc/3f9f9888-f7bb-453d-ae8b-86c63e78f196)
- [FDA Inspection 762880 - 2012-01-12](https://www.keypedia.com/records/fda_inspections/vortek-surgical-llc/185124ae-7669-47b7-99fc-36d792597fa3)

Company: https://www.keypedia.com/companies/vortek-surgical-llc/8a117fe3-7998-4790-a99a-3ce1a6ae1476

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