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FDA Inspection 629562 — Allermed Laboratories, Inc.

Allermed Laboratories, Inc. — FEI 1000098920

The FDA completed an inspection of Allermed Laboratories, Inc. on November 13, 2009 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
November 13, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Diego, CA (United States)

Facility

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FDA data resources