FDA Inspection 764701 — Vida Diagnostics, Inc.

Vida Diagnostics, Inc. — FEI 3007233544

The FDA completed an inspection of Vida Diagnostics, Inc. on Jan 25, 2012 in Coralville, IA. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 25, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Coralville, IA (United States)

Citations

IDCFRDescription
323221 CFR 820.72(a)Equipment suitability & capability
342621 CFR 820.50(a)(1)Documented evaluation