FDA Inspection 978933 — Produits Dentaires Pierre Rolland

Produits Dentaires Pierre Rolland — FEI 3003677417

The FDA completed an inspection of Produits Dentaires Pierre Rolland on June 16, 2016 in Merignac. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 16, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Merignac (France)