# FDA Inspection 638742 - OrthoPlus Inc - January 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/orthoplus-inc/b947e5bf-ef72-4d0f-9816-cb11ffb69117
Source feed: FDA_Inspections

> FDA Inspection 638742 for OrthoPlus Inc on January 15, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 638742
- Company Name: OrthoPlus Inc
- Inspection Date: 2010-01-15
- Classification: Voluntary Action Indicated (VAI)
- 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/orthoplus-inc/77a4907b-20fc-41d4-b2d3-8bd339218bd3

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