# FDA Inspection 989319 - Osteometer MediTech  Inc - February 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/osteometer-meditech-inc/a6bf5dc3-d262-47b0-abfb-72e8b554de8c
Source feed: FDA_Inspections

> FDA Inspection 989319 for Osteometer MediTech  Inc on February 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989319
- Company Name: Osteometer MediTech  Inc
- Inspection Date: 2016-02-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 854160 - 2013-09-09](https://www.keypedia.com/records/fda_inspections/osteometer-meditech-inc/ac171ede-9b5f-4d6a-b592-1cc8f68b7928)
- [FDA Inspection 612808 - 2009-07-08](https://www.keypedia.com/records/fda_inspections/osteometer-meditech-inc/650527b4-772c-4dcf-a9bf-9eec09d254d0)

Company: https://www.keypedia.com/companies/osteometer-meditech-inc/f5dc18ee-729d-4b26-a53d-6d139788b237

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