# Osteometer MediTech  Inc – FDA Inspection, Feb 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 of Osteometer MediTech  Inc, February 19, 2016. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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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)
- 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

## Related Documents

- FDA Inspection 854160 - 2013-09-09
- FDA Inspection 612808 - 2009-07-08

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