# FDA Inspection 1052182 - Osteomedix Inc - April 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/osteomedix-inc/c2df167b-cc2b-4936-92d7-eed95cfe9b99
Source feed: FDA_Inspections

> FDA Inspection 1052182 for Osteomedix Inc on April 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052182
- Company Name: Osteomedix Inc
- Inspection Date: 2018-04-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1052182 - 2018-04-27](https://www.globalkeysolutions.net/records/fda_inspections/osteomedix-inc/866a457d-ee13-4a40-8a01-c5c7380f9aba)

Company: https://www.globalkeysolutions.net/companies/osteomedix-inc/eacd784a-57f9-4167-ab3a-5b5f45ebae51

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