# FDA Inspection 1027565 - Synvasive Technology, Inc. - May 04, 2017

Source: https://www.keypedia.com/records/fda_inspections/synvasive-technology-inc/e24ae3bd-afd8-4b28-9be5-d5db03c5a922
Source feed: FDA_Inspections

> FDA Inspection 1027565 for Synvasive Technology, Inc. on May 04, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027565
- Company Name: Synvasive Technology, Inc.
- Inspection Date: 2017-05-04
- 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 1027565 - 2017-05-04](https://www.keypedia.com/records/fda_inspections/synvasive-technology-inc/76d77e8a-ce7f-4904-b498-2341a660432a)
- [FDA Inspection 888903 - 2014-06-19](https://www.keypedia.com/records/fda_inspections/synvasive-technology-inc/7a07ccad-95d2-4506-9885-37c6af48a414)
- [FDA Inspection 888903 - 2014-06-19](https://www.keypedia.com/records/fda_inspections/synvasive-technology-inc/bc278256-4b2a-4901-a8dc-6a9bd3639ce8)

Company: https://www.keypedia.com/companies/synvasive-technology-inc/399f3c7e-92d3-413a-9d2a-76b77e0c96b6

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