# FDA Inspection 1068829 - HMD Biomedical Inc. - August 30, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/hmd-biomedical-inc/5340b5e8-def6-41e1-95b5-d40d0cfb9a23
Source feed: FDA_Inspections

> FDA Inspection 1068829 for HMD Biomedical Inc. on August 30, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1068829
- Company Name: HMD Biomedical Inc.
- Inspection Date: 2018-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1068829 - 2018-08-30](https://www.globalkeysolutions.net/records/fda_inspections/hmd-biomedical-inc/eff377e1-c95a-46e8-983f-c85fd235ecbb)
- [FDA Inspection 965362 - 2016-03-31](https://www.globalkeysolutions.net/records/fda_inspections/hmd-biomedical-inc/75e550a0-87b1-444a-b6a7-4a9394c99f5e)

Company: https://www.globalkeysolutions.net/companies/hmd-biomedical-inc/2c0dedba-6f8b-42d3-aa46-0d1ef7a86550

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