# Anchor Products Company, Inc. – FDA Inspection, Jun 4, 2010

Source: https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/fab3a09c-e8c0-4303-96a0-9f5c35e6e3d4
Source feed: FDA_Inspections

> FDA inspection 666324 of Anchor Products Company, Inc., June 04, 2010. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 666324
- Company Name: Anchor Products Company, Inc.
- Inspection Date: 2010-06-04
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 985552 - 2016-09-26
- [FDA Inspection 854186 - 2013-10-25](https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/f59a260f-1a9a-4ba8-adcd-bc9b6878baec)
- [FDA Inspection 725032 - 2011-05-12](https://www.keypedia.com/records/fda_inspections/anchor-products-company-inc/61e625ea-0d47-47de-a43b-59e6d7f6db94)

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