FDA Inspection 1009104 — Zyppah Inc.

Zyppah Inc. — FEI 3013269322

The FDA completed an inspection of Zyppah Inc. on Mar 15, 2017 in Calabasas, CA. 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
Mar 15, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Calabasas, CA (United States)

Citations

IDCFRDescription
317021 CFR 820.198(b)Review and evaluation for investigation

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