# FDA Inspection 1055504 - taberna pro medicum - June 14, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/taberna-pro-medicum/2f4766a2-71c6-41f0-9366-5d9b01566649
Source feed: FDA_Inspections

> FDA Inspection 1055504 for taberna pro medicum on June 14, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055504
- Company Name: taberna pro medicum
- Inspection Date: 2018-06-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 808669 - 2012-11-01](https://www.globalkeysolutions.net/records/fda_inspections/taberna-pro-medicum/590eb90a-1b85-4821-a5ae-81096fd48e54)

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