FDA Inspection 1016285 — Maxim Biomedical Inc.

Maxim Biomedical Inc. — FEI 1122236

The FDA completed an inspection of Maxim Biomedical Inc. on May 18, 2017 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 18, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rockville, MD (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.