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FDA Inspection 843070 — Allermed Laboratories, Inc.

Allermed Laboratories, Inc. — FEI 1000098920

The FDA completed an inspection of Allermed Laboratories, Inc. on August 12, 2013 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
August 12, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Diego, CA (United States)

Facility

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FDA data resources