# taberna pro medicum – FDA Inspection, Jun 14, 2018

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

> FDA inspection 1055504 of taberna pro medicum, June 14, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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

## Related Documents

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

## Related Officers

- [Company Rep](https://www.keypedia.com/people/amanda-dinaro/6df79979-ad5c-46f5-8917-197f8a0870e0)

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

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