FDA Inspection 994520 — Kent Laboratories, Inc.

Kent Laboratories, Inc. — FEI 3019906

The FDA completed an inspection of Kent Laboratories, Inc. on Dec 7, 2016 in Bellingham, WA. 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.