# FDA Inspection 985992 - Orthomerica Products, Inc. - August 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/971e74b3-e1b7-4ca6-a990-710bbe103506
Source feed: FDA_Inspections

> FDA Inspection 985992 for Orthomerica Products, Inc. on August 26, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985992
- Company Name: Orthomerica Products, Inc.
- Inspection Date: 2016-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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 985992 - 2016-08-26](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/d0989fa8-4020-4e9c-a005-f615b39c1e88)
- [FDA Inspection 830911 - 2013-05-07](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/8ce56b30-48cb-4216-9318-fa7398b0e234)
- [FDA Inspection 830911 - 2013-05-07](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/88279a4f-98ca-4ebb-9a18-d8e251d1f545)
- [FDA Inspection 611156 - 2009-09-10](https://www.keypedia.com/records/fda_inspections/orthomerica-products-inc/9c6c01af-0f85-4bd6-8c04-914e3c812546)

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