# HMD Biomedical Inc. – FDA Inspection, Aug 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/hmd-biomedical-inc/eff377e1-c95a-46e8-983f-c85fd235ecbb
Source feed: FDA_Inspections

> FDA inspection 1068829 of HMD Biomedical Inc., August 30, 2018. Classification: No Action Indicated (NAI). Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1068829
- Company Name: HMD Biomedical Inc.
- Inspection Date: 2018-08-30
- 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 1025683 - 2017-07-05](https://www.keypedia.com/records/fda_inspections/hmd-biomedical-inc/5ab233fc-640d-4408-8a27-dd4fccca1771)
- [FDA Inspection 965362 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/hmd-biomedical-inc/75e550a0-87b1-444a-b6a7-4a9394c99f5e)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

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

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