# Mauna Kea Technologies – FDA Inspection, May 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/mauna-kea-technologies/5f3cf109-b885-402a-aee4-6374ce63eb64
Source feed: FDA_Inspections

> FDA inspection 1053547 of Mauna Kea Technologies, May 17, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053547
- Company Name: Mauna Kea Technologies
- Inspection Date: 2018-05-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- 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 1247593 - 2024-07-04
- FDA Inspection 865535 - 2014-01-30

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/mauna-kea-technologies/dd04702e-623c-4805-b12c-a130ec0da965

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