# Viant Upland, Inc. – FDA Inspection, Nov 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/viant-upland-inc/656ecf1b-4092-4a94-aa69-b913041e1725
Source feed: FDA_Inspections

> FDA inspection 1223351 of Viant Upland, Inc., November 16, 2023. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223351
- Company Name: Viant Upland, Inc.
- Inspection Date: 2023-11-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 881549 - 2014-05-22](https://www.keypedia.com/records/fda_inspections/viant-upland-inc/5ab49625-e99c-4914-be16-f4ab50b51ffa)
- FDA Inspection 728836 - 2011-05-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/marlo-ian-m-alintanahin/a37da927-b369-4753-b275-41743556f25e)

Company: https://www.keypedia.com/companies/viant-upland-inc/bfd3e83b-13fb-4dc1-86a8-3cb893ce2f59

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