FDA Inspection 754968 — bioLytical Laboratories, Inc.

bioLytical Laboratories, Inc. — FEI 3003871407

The FDA completed an inspection of bioLytical Laboratories, Inc. on Nov 11, 2011 in Richmond. 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
Nov 11, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Richmond (Canada)

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