FDA Inspection 759639 — Lingraphicare America, Inc.

Lingraphicare America, Inc. — FEI 1000123978

The FDA completed an inspection of Lingraphicare America, Inc. on December 21, 2011 in Princeton, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 21, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Princeton, NJ (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation