# ZEPHYR SLEEP TECHNOLOGIES INC. – FDA Inspection, Dec 8, 2015

Source: https://www.keypedia.com/records/fda_inspections/zephyr-sleep-technologies-inc/7b71aa19-ffd5-4e3e-a4e2-da1113d2ce2f
Source feed: FDA_Inspections

> FDA inspection 953840 of ZEPHYR SLEEP TECHNOLOGIES INC., December 08, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953840
- Company Name: ZEPHYR SLEEP TECHNOLOGIES INC.
- Inspection Date: 2015-12-08
- 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: 3

## Related Documents

- [FDA Inspection 1141388 - 2019-06-26](https://www.keypedia.com/records/fda_inspections/zephyr-sleep-technologies-inc/5fa9cd93-fb78-4eaa-aa03-b4bf8e1fa7ea)

Company: https://www.keypedia.com/companies/zephyr-sleep-technologies-inc/a33bb5bd-0207-4776-958c-7b22da0d9365

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