# Osteotech, Inc. – FDA Inspection, Aug 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/osteotech-inc/7f0db1ef-b91e-4473-b0a5-2bff6aaaaf6e
Source feed: FDA_Inspections

> FDA inspection 845698 of Osteotech, Inc., August 16, 2013. Classification: No Action Indicated (NAI). 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 845698
- Company Name: Osteotech, Inc.
- Inspection Date: 2013-08-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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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-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7