FDA Inspection 800940 — Brooklands, Inc.

Brooklands, Inc. — FEI 3003859288

The FDA completed an inspection of Brooklands, Inc. on Sep 14, 2012 in Boca Raton, 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
Sep 14, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Boca Raton, FL (United States)