Home / Inspections / 952980

FDA Inspection 952980 — Maxim Biomedical Inc.

Maxim Biomedical Inc. — FEI 1122236

The FDA completed an inspection of Maxim Biomedical Inc. on December 1, 2015 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 1, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Rockville, MD (United States)

Facility

Other inspections at this facility

  • 1270828 (NAI Wed May 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1222136 (NAI Thu Nov 02 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1084838 (NAI Thu Feb 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068675 (NAI Tue Sep 18 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1016285 (NAI Thu May 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources