# FDA Inspection 808669 - taberna pro medicum - November 01, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/taberna-pro-medicum/590eb90a-1b85-4821-a5ae-81096fd48e54
Source feed: FDA_Inspections

> FDA Inspection 808669 for taberna pro medicum on November 01, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808669
- Company Name: taberna pro medicum
- Inspection Date: 2012-11-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055504 - 2018-06-14](https://www.globalkeysolutions.net/records/fda_inspections/taberna-pro-medicum/2f4766a2-71c6-41f0-9366-5d9b01566649)

Company: https://www.globalkeysolutions.net/companies/taberna-pro-medicum/f87a6982-eff1-470c-b003-f4477e885173

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