# Denali R & D Corporation – FDA Inspection, Jul 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/denali-r-d-corporation/373f916c-44f1-458b-abd8-464c3f399718
Source feed: FDA_Inspections

> FDA inspection 1017929 of Denali R & D Corporation, July 12, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 1017929
- Company Name: Denali R & D Corporation
- Inspection Date: 2017-07-12
- 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: 1

## Related Documents

- FDA Inspection 1154255 - 2021-10-06
- FDA Inspection 785239 - 2012-06-01

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-p-finn/70e5c36c-2711-449b-bf73-e08b4dd58449)

Company: https://www.keypedia.com/companies/denali-r-d-corporation/5a00647c-133e-42a5-a847-b2c57f59c89a

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