Benchmark Electronics (BE), an integrated electronics manufacturing services (EMS) provider, has reported that its Thailand facility has completed a full Quality System Inspection Technique (QSIT) audit from the Food and Drug Administration (FDA).

BE said that the audit was completed through the company’s premarket approval (PMA) supplement evaluation process, to manufacture Class III finished medical devices on behalf of large tier-one medical original equipment manufacturers (OEMs).

Benchmark Electronics CEO Cary Fu said that he was pleased to announce the addition of Class III medical device capabilities in Asia and said that with the capability they expand the level and scope of delivering excellent product solutions to medical equipment manufacturers.

“Our Class III medical device manufacturing in Thailand supplements Benchmark’s other recently expanded service offerings worldwide, which includes precision technologies and increased design engineering depth,” Fu said.