# Agendia, Inc. – FDA Inspection, Aug 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/agendia-inc/ce84f4ee-8b75-46a9-8808-a4fc6cbad512
Source feed: FDA_Inspections

> FDA inspection 1022495 of Agendia, Inc., August 22, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022495
- Company Name: Agendia, Inc.
- Inspection Date: 2017-08-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

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- FDA Inspection 1167584 - 2022-04-12
- FDA Inspection 747287 - 2011-08-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kirtida-patel/c62852cf-9724-4296-bc4b-de8993dcf716)

Company: https://www.keypedia.com/companies/agendia-inc/3f132159-b8a0-4c5c-be76-3023266dde9b

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