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FDA Inspection 947983 — Greer Laboratories, Inc.

Greer Laboratories, Inc. — FEI 1011574

The FDA completed an inspection of Greer Laboratories, Inc. on August 27, 2015 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
August 27, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Lenoir, NC (United States)

Facility

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  • 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))
  • 1036168 (VAI Wed Nov 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1014272 (VAI Thu Jun 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources