FDA Inspection 697737 — R82 A/S

R82 A/S — FEI 3001657382

The FDA completed an inspection of R82 A/S on Oct 7, 2010 in Gedved. 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). Product area: Devices.