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 or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 1, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Islandia, NY (United States)

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