# Osteotech, Inc. – FDA Inspection, Aug 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/osteotech-inc/e4a403d7-328b-4e7c-a1de-3e59c35cb327
Source feed: FDA_Inspections

> FDA inspection 1021037 of Osteotech, Inc., August 10, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 1271. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021037
- Company Name: Osteotech, Inc.
- Inspection Date: 2017-08-10
- 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: 3

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- [FDA Inspection 1060874 - 2018-07-30](https://www.keypedia.com/records/fda_inspections/osteotech-inc/53653e50-b1c2-439f-9985-fa3c1388351b)
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## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)
- [Company Rep](https://www.keypedia.com/people/jennifer-l-custodio/489a8b9c-ab8d-4d37-b89c-6086889e825c)
- [Company Rep](https://www.keypedia.com/people/sarah-m-forney/3d68a56a-3c2f-4606-8e98-03808281842b)

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