FDA Warning Letter — Genus Lifesciences Inc.

Case 174813 — FEI 3003851100

The FDA took a Warning Letter action against Genus Lifesciences Inc. on Jul 15, 2011 (Allentown, PA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Genus Lifesciences Inc.
Date
Jul 15, 2011
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
Allentown, PA (United States)

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