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FDA Inspection 927931 — Permobil Inc

Permobil Inc — FEI 1221084

The FDA completed an inspection of Permobil Inc on May 28, 2015 in Lebanon, TN. 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
May 28, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Lebanon, TN (United States)

Facility

Other inspections at this facility

  • 1149139 (VAI Tue Aug 17 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037821 (NAI Thu Jan 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768863 (VAI Thu Feb 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 599948 (NAI Tue Jul 21 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources