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FDA Inspection 815890 — Maxim Biomedical Inc.

Maxim Biomedical Inc. — FEI 1122236

The FDA completed an inspection of Maxim Biomedical Inc. on December 7, 2012 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 7, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Rockville, MD (United States)

Facility

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FDA data resources