FDA Inspection 1073444 — Genus Lifesciences Inc.

Genus Lifesciences Inc. — FEI 3003851100

The FDA completed an inspection of Genus Lifesciences Inc. on Nov 28, 2018 in Allentown, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Nov 28, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Allentown, PA (United States)

Additional details

Postmarket Adverse Drug Experience (PADE)

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