FDA Inspection 1071623 — Anuncia, Inc.

Anuncia, Inc. — FEI 3014522419

The FDA completed an inspection of Anuncia, Inc. on November 14, 2018 in Scottsdale, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 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