FDA Inspection 1071623 — Anuncia, Inc.

Anuncia, Inc. — FEI 3014522419

The FDA completed an inspection of Anuncia, Inc. on Nov 14, 2018 in Scottsdale, AZ. 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
Nov 14, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Scottsdale, AZ (United States)

Citations

IDCFRDescription
312821 CFR 820.90(a)Nonconforming product control

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