FDA Inspection 761459 — Invivo Corporation

Invivo Corporation — FEI 1000113495

The FDA completed an inspection of Invivo Corporation on Dec 16, 2011 in Gainesville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 16, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Gainesville, FL (United States)

Citations

IDCFRDescription
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures