# Ambi, Inc – FDA Inspection, Dec 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/ambi-inc/311ce946-dac4-408d-b235-81d0da811bf0
Source feed: FDA_Inspections

> FDA inspection 1035272 of Ambi, Inc, December 14, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035272
- Company Name: Ambi, Inc
- Inspection Date: 2017-12-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1272791 - 2025-06-13](https://www.keypedia.com/records/fda_inspections/ambi-inc/a6a0b628-bed1-456a-adbf-e382981d16ac)
- FDA Inspection 1163119 - 2022-02-16

## Related Officers

- Issuing Officer

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