FDA Inspection 996259 — Rhinosystems Inc

Rhinosystems Inc — FEI 3007644779

The FDA completed an inspection of Rhinosystems Inc on Dec 2, 2016 in Brooklyn, OH. 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
Dec 2, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn, OH (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures

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