FDA Inspection 683180 — Kent Laboratories, Inc.

Kent Laboratories, Inc. — FEI 3019906

The FDA completed an inspection of Kent Laboratories, Inc. on Sep 21, 2010 in Bellingham, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Bellingham, WA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.