# FDA Inspection 960831 - Surgistar, Inc. - January 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/surgistar-inc/a191dfd6-7958-4f2f-8954-cb978adc0268
Source feed: FDA_Inspections

> FDA Inspection 960831 for Surgistar, Inc. on January 26, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960831
- Company Name: Surgistar, Inc.
- Inspection Date: 2016-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 816842 - 2012-12-18](https://www.keypedia.com/records/fda_inspections/surgistar-inc/32b4557c-a476-4ae0-a959-2dac29cda56d)
- [FDA Inspection 816842 - 2012-12-18](https://www.keypedia.com/records/fda_inspections/surgistar-inc/c9aab7cc-bfb8-4395-80aa-0d63a925dc24)

Company: https://www.keypedia.com/companies/surgistar-inc/0ef058c0-5166-4a93-80e3-f90bee4ae1c4

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