# Geneva Laboratories, Inc – FDA Inspection, Apr 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/geneva-laboratories-inc/89670481-1746-4c31-b7e2-d64325a53de0
Source feed: FDA_Inspections

> FDA inspection 1046966 of Geneva Laboratories, Inc, April 05, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 58. Form 483 issued. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1046966
- Company Name: Geneva Laboratories, Inc
- Inspection Date: 2018-04-05
- 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 Documents

- [FDA Inspection 1290960 - 2025-11-04](https://www.keypedia.com/records/fda_inspections/geneva-laboratories-inc/b95f90f3-14b6-420d-98a1-1e142083dfb3)
- FDA Inspection 1143396 - 2021-06-03
- FDA Inspection 930535 - 2015-06-11
- FDA Inspection 761091 - 2011-12-30
- FDA Inspection 664201 - 2010-05-06

## Related Officers

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

Company: https://www.keypedia.com/companies/geneva-laboratories-inc/f06d802f-33ba-4e22-8fba-667d97ec0721

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