# Orthomerica Products, Inc. – FDA Inspection, Sep 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/9c6c01af-0f85-4bd6-8c04-914e3c812546
Source feed: FDA_Inspections

> FDA inspection 611156 of Orthomerica Products, Inc., September 10, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611156
- Company Name: Orthomerica Products, Inc.
- Inspection Date: 2009-09-10
- 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 985992 - 2016-08-26](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/f61317e3-6255-4a80-85ed-dea8d0b3796f)
- [FDA Inspection 830911 - 2013-05-07](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/8ce56b30-48cb-4216-9318-fa7398b0e234)

Company: https://www.keypedia.com/companies/orthomerica-products-inc/17659eeb-6a5a-4d49-a7e0-d21b287a20f2

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