# Osteomed, LLC – FDA Inspection, Sep 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/osteomed-llc/cce3738e-e82a-435b-9f7d-be72d6637cc2
Source feed: FDA_Inspections

> FDA inspection 1026378 of Osteomed, LLC, September 22, 2017. Classification: No Action Indicated (NAI). 6 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026378
- Company Name: Osteomed, LLC
- Inspection Date: 2017-09-22
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

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- [FDA Inspection 955878 - 2016-01-07](https://www.keypedia.com/records/fda_inspections/osteomed-llc/47e43609-507a-42d7-84b1-44170e97322d)
- FDA Inspection 868667 - 2014-02-28

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/ellen-j-tave/a70cd3ed-957f-471b-82ff-24ca7c65bc10)

Company: https://www.keypedia.com/companies/osteomed-llc/4b0582e3-14ed-4c50-b81e-eddb941a5531

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7