FDA Inspection 939089 — Demetech Corp.

Demetech Corp. — FEI 3003063934

The FDA completed an inspection of Demetech Corp. on Aug 26, 2015 in Miami Lakes, FL. 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.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Miami Lakes, FL (United States)