# Vertebral Technologies, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vertebral-technologies-inc/136ed3a9-e2ed-492a-9c70-30d12953740f

> Inspection records and compliance data for Vertebral Technologies, Inc. in Santa Clara, California. Access full analysis and detailed observations.

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## Details

- Name: Vertebral Technologies, Inc.
- FEI Number: 3007617183
- City: Santa Clara
- State: California
- Country Name: United States
- Address Line 1: 2344 Walsh Ave
- Zip Code: 95051

## Related Documents

- [FDA Inspection 994689 - Vertebral Technologies, Inc. - 2016-11-16](https://www.globalkeysolutions.net/records/fda_inspections/vertebral-technologies-inc/91b487da-9ff3-434c-bdef-4c7428d5be70) — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2016
- [WARNING_LETTER - Vertebral Technologies, Inc. - 2015-02-02](https://www.globalkeysolutions.net/records/warning_letter/vertebral-technologies-inc/ae455398-74d0-495b-b0b4-a742bfd2f318) — source: FDA, date: February 2, 2015
- [FDA Inspection 912320 - Vertebral Technologies, Inc. - 2015-02-02](https://www.globalkeysolutions.net/records/fda_inspections/vertebral-technologies-inc/4e21fed2-8b41-450a-a86d-b1876a004bad) — classification: Official Action Indicated (OAI), source: FDA, date: February 2, 2015
- [FDA Inspection 776625 - Vertebral Technologies, Inc. - 2012-04-16](https://www.globalkeysolutions.net/records/fda_inspections/vertebral-technologies-inc/f2d27272-ce3f-4674-8c41-b29c711d1dee) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2012
- [FDA Inspection 776625 - Vertebral Technologies, Inc. - 2012-04-16](https://www.globalkeysolutions.net/records/fda_inspections/vertebral-technologies-inc/04940181-b650-4903-b6d2-68f5e377c5b4) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2012
- [FDA Inspection 588231 - Vertebral Technologies, Inc. - 2009-06-12](https://www.globalkeysolutions.net/records/fda_inspections/vertebral-technologies-inc/86629c03-54c7-4acd-9243-e1c7afe531de) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2009

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## Related Officers

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