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FDA Inspection 1059881 — Navajo Manufacturing Company, Inc.

Navajo Manufacturing Company, Inc. — FEI 3006140792

The FDA completed an inspection of Navajo Manufacturing Company, Inc. on July 18, 2018 in Denver, CO. 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
July 18, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Denver, CO (United States)

Facility

Other inspections at this facility

  • 1306638 (VAI Thu Mar 05 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1065492 (NAI Tue Jul 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources