# FDA Inspection 980305 - Surgistar Inc - August 05, 2016

Source: https://www.keypedia.com/records/fda_inspections/surgistar-inc/c60b8b3e-98c4-4698-b227-e932c8eb9e97
Source feed: FDA_Inspections

> FDA Inspection 980305 for Surgistar Inc on August 05, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980305
- Company Name: Surgistar Inc
- Inspection Date: 2016-08-05
- 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 980305 - 2016-08-05](https://www.keypedia.com/records/fda_inspections/surgistar-inc/940036f8-22ea-4bf0-83ca-c167dbf416f1)
- [FDA Inspection 815299 - 2012-12-12](https://www.keypedia.com/records/fda_inspections/surgistar-inc/59084c34-9999-4f3c-b9d9-2ba6f95cc0c0)
- [FDA Inspection 732565 - 2011-06-30](https://www.keypedia.com/records/fda_inspections/surgistar-inc/6f0414ca-c562-492f-acfc-c3245089c9d1)

Company: https://www.keypedia.com/companies/surgistar-inc/1254820d-17b0-4f84-abce-e03e3570c727

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