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FDA Inspection 1036168 — Greer Laboratories, Inc.

Greer Laboratories, Inc. — FEI 1011574

The FDA completed an inspection of Greer Laboratories, Inc. on November 22, 2017 in Lenoir, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

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

Facility

Other inspections at this facility

  • 1256993 (VAI Wed Dec 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1182373 (NAI Tue Nov 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102216 (VAI Wed Sep 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1014272 (VAI Thu Jun 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 947983 (VAI Thu Aug 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources