# InBios International, Inc. – FDA Inspection, Aug 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/inbios-international-inc/8386e279-fd78-4cf4-98cc-3d445136c215
Source feed: FDA_Inspections

> FDA inspection 1064523 of InBios International, Inc., August 23, 2018. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064523
- Company Name: InBios International, Inc.
- Inspection Date: 2018-08-23
- 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: 4

## Related Documents

- FDA Inspection 1172098 - 2022-06-16
- FDA Inspection 927383 - 2015-05-15
- [FDA Inspection 827548 - 2013-04-22](https://www.keypedia.com/records/fda_inspections/inbios-international-inc/c5e185cd-0c8f-441d-8ed3-c116f720c872)
- FDA Inspection 779697 - 2012-05-04
- FDA Inspection 683144 - 2010-08-27

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/inbios-international-inc/a521a8a5-8c79-4dab-bf12-84f73b18961b

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