FDA Inspection 788842 — Innovia Llc

Innovia Llc — FEI 3004444223

The FDA completed an inspection of Innovia Llc on Jun 22, 2012 in Miami, FL. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
312321 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures