FDA Inspection 1036168 — Greer Laboratories, Inc.

Greer Laboratories, Inc. — FEI 1011574

The FDA completed an inspection of Greer Laboratories, Inc. on Nov 22, 2017 in Lenoir, NC. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 22, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Lenoir, NC (United States)

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