# Surpass, Inc. – FDA Inspection, Dec 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/surpass-inc/90167850-3757-47ac-93a9-a8ddfe988aa8
Source feed: FDA_Inspections

> FDA inspection 1034099 of Surpass, Inc., December 07, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 58. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034099
- Company Name: Surpass, Inc.
- Inspection Date: 2017-12-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 4

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/denise-l-burosh/075a442f-67e0-4a65-9c09-e8819a329773)

Company: https://www.keypedia.com/companies/surpass-inc/adeae37b-db03-49f9-8022-816e5c02ee00

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d