# Osteotech, Inc. – FDA Inspection, Dec 9, 2010

Source: https://www.keypedia.com/records/fda_inspections/osteotech-inc/9f6749e0-b853-4c18-aff4-5e53a09fd384
Source feed: FDA_Inspections

> FDA inspection 699572 of Osteotech, Inc., December 09, 2010. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 806, 820 and 1271. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 699572
- Company Name: Osteotech, Inc.
- Inspection Date: 2010-12-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 10

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- [FDA Inspection 1150237 - 2021-08-12](https://www.keypedia.com/records/fda_inspections/osteotech-inc/5d361e25-cf2a-4c5e-8652-100402b95bc5)
- [FDA Inspection 1060874 - 2018-07-30](https://www.keypedia.com/records/fda_inspections/osteotech-inc/53653e50-b1c2-439f-9985-fa3c1388351b)
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- FDA Inspection 925160 - 2015-05-06

Company: https://www.keypedia.com/companies/osteotech-inc/916ecda8-a52b-4078-aadc-eaee17461f83

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