FDA Inspection 850450 — Nuvolase Inc.

Nuvolase Inc. — FEI 3007590700

The FDA completed an inspection of Nuvolase Inc. on September 20, 2013 in Los Angeles, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
1471621 CFR 820.30(f)Design verification - output does not meet input requirement
313021 CFR 820.100(a)Lack of or inadequate procedures
320621 CFR 820.50(b)Approval, inadequate purchasing data