# Andersen Products, Inc. – FDA Inspection, Jul 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/andersen-products-inc/e115e71e-2128-4e52-b4fb-2d7d615f0b3b
Source feed: FDA_Inspections

> FDA inspection 1017867 of Andersen Products, Inc., July 14, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017867
- Company Name: Andersen Products, Inc.
- Inspection Date: 2017-07-14
- 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: 3

## Related Documents

- [FDA Inspection 774266 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/andersen-products-inc/60433681-191d-4a75-a12d-b1dda75370ad)

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

Company: https://www.keypedia.com/companies/andersen-products-inc/be527d93-fb1a-40ad-a94f-24a7346ace26

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