# Transoma Medical – FDA Inspection, Aug 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/transoma-medical/fe4ebbd3-3669-437f-8fc3-c63b7755d241
Source feed: FDA_Inspections

> FDA inspection 606323 of Transoma Medical, August 28, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 606323
- Company Name: Transoma Medical
- Inspection Date: 2009-08-28
- 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: 2

Company: https://www.keypedia.com/companies/transoma-medical/e70112f4-b982-434a-a33d-0f6356c20dae

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