# FDA Inspection 556415 - Vertebron Inc - January 13, 2009

Source: https://www.keypedia.com/records/fda_inspections/vertebron-inc/7064e54a-262c-4633-87b1-c094602ababf
Source feed: FDA_Inspections

> FDA Inspection 556415 for Vertebron Inc on January 13, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 556415
- Company Name: Vertebron Inc
- Inspection Date: 2009-01-13
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

Company: https://www.keypedia.com/companies/vertebron-inc/8c0fa0f8-8887-4e41-b245-4ada4bde548a

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d