# Electromedical Products International, Inc. – FDA Inspection, Dec 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/electromedical-products-international-inc/a22b6f7c-868b-4902-92cb-cf325c7d3fd5
Source feed: FDA_Inspections

> FDA inspection 636051 of Electromedical Products International, Inc., December 18, 2009. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 636051
- Company Name: Electromedical Products International, Inc.
- Inspection Date: 2009-12-18
- 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: 9

## Related Documents

- [FDA Inspection 1039669 - 2018-02-02](https://www.keypedia.com/records/fda_inspections/electromedical-products-international-inc/fcfd53c2-c923-4caa-866d-7d6be0c8a9ab)
- FDA Inspection 863799 - 2014-01-29
- [FDA Inspection 816802 - 2013-02-01](https://www.keypedia.com/records/fda_inspections/electromedical-products-international-inc/d86bf5a8-2727-4598-862e-a379726392f6)

Company: https://www.keypedia.com/companies/electromedical-products-international-inc/92c6e4f2-4e3c-4c0e-8c26-d059cf43145b

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