# FDA Inspection 1017867 - Andersen Products, Inc. - July 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 for Andersen Products, Inc. on July 14, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1017867
- Company Name: Andersen Products, Inc.
- Inspection Date: 2017-07-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1017867 - 2017-07-14](https://www.keypedia.com/records/fda_inspections/andersen-products-inc/6b447c5d-c107-4619-b274-04c62d967c17)
- [FDA Inspection 774266 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/andersen-products-inc/14b32c87-53fb-4aba-a193-4793c3b8611d)
- [FDA Inspection 774266 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/andersen-products-inc/60433681-191d-4a75-a12d-b1dda75370ad)

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