# Anchor Products Company, Inc. – FDA Inspection, Oct 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/f59a260f-1a9a-4ba8-adcd-bc9b6878baec
Source feed: FDA_Inspections

> FDA inspection 854186 of Anchor Products Company, Inc., October 25, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 854186
- Company Name: Anchor Products Company, Inc.
- Inspection Date: 2013-10-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 985552 - 2016-09-26
- [FDA Inspection 725032 - 2011-05-12](https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/61e625ea-0d47-47de-a43b-59e6d7f6db94)
- [FDA Inspection 666324 - 2010-06-04](https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/fab3a09c-e8c0-4303-96a0-9f5c35e6e3d4)

Company: https://www.keypedia.com/companies/anchor-products-company-inc/a2661d2f-0ea3-49c8-8865-02fed7a17eb9

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