# FDA Inspection 1035272 - Ambi, Inc - December 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/ambi-inc/158bfa8e-7bba-4122-b3fd-19cefcd822ed
Source feed: FDA_Inspections

> FDA Inspection 1035272 for Ambi, Inc on December 14, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035272
- Company Name: Ambi, Inc
- Inspection Date: 2017-12-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ambi-inc/801c6331-b8f5-4a5b-8551-16ff53b77acb

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