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FDA Inspection 1022877 — Allermed Laboratories, Inc.

Allermed Laboratories, Inc. — FEI 1000098920

The FDA completed an inspection of Allermed Laboratories, Inc. on June 14, 2017 in San Diego, CA. 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
June 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Diego, CA (United States)

Facility

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  • 1071500 (VAI Mon Nov 12 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933388 (VAI Mon Jul 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 843070 (VAI Mon Aug 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 749646 (VAI Tue Sep 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources