FDA Inspection 1055504 — Taberna Pro Medicum

Taberna Pro Medicum — FEI 3000311264

The FDA completed an inspection of Taberna Pro Medicum on Jun 14, 2018 in Luneburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Luneburg (Germany)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
317021 CFR 820.198(b)Review and evaluation for investigation