# Danmar Products, Inc. – FDA Inspection, Jan 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/danmar-products-inc/fc5df629-0dc7-4163-a632-5a7b96f16d2e
Source feed: FDA_Inspections

> FDA inspection 554943 of Danmar Products, Inc., January 15, 2009. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 554943
- Company Name: Danmar Products, Inc.
- Inspection Date: 2009-01-15
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

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- [FDA Inspection 1252815 - 2024-11-04](https://www.keypedia.com/records/fda_inspections/danmar-products-inc/4588e133-3b3b-426a-bce3-9fe6a1525814)
- [FDA Inspection 1032276 - 2017-11-15](https://www.keypedia.com/records/fda_inspections/danmar-products-inc/a567f7d0-7b6e-494f-9892-6b3bfdd48e6d)
- FDA Inspection 901058 - 2014-10-30
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- FDA Inspection 658929 - 2010-04-12

Company: https://www.keypedia.com/companies/danmar-products-inc/e0efaa09-c225-4b86-8eb8-60e7903e3e89

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