FDA Inspection 1047534 — Flexbar Machine Corp

Flexbar Machine Corp — FEI 2424366

The FDA completed an inspection of Flexbar Machine Corp on Apr 4, 2018 in Islandia, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 4, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Islandia, NY (United States)

Citations

IDCFRDescription
50221 CFR 820.60Identification procedures, Lack of or inadequate procedures

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