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FDA Inspection 779265 — Flexbar Machine Corp

Flexbar Machine Corp — FEI 2424366

The FDA completed an inspection of Flexbar Machine Corp on May 1, 2012 in Islandia, NY. 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 1, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Islandia, NY (United States)

Facility

Other inspections at this facility

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  • 1047534 (VAI Wed Apr 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 888627 (NAI Tue Jul 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 625749 (VAI Fri Oct 30 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources