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FDA Inspection 697772 — Maxim Biomedical Inc.

Maxim Biomedical Inc. — FEI 1122236

The FDA completed an inspection of Maxim Biomedical Inc. on October 19, 2010 in Rockville, MD. 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
October 19, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rockville, MD (United States)

Facility

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FDA data resources