FDA Inspection 671807 — Replication Medical, Inc.

Replication Medical, Inc. — FEI 3004641714

The FDA completed an inspection of Replication Medical, Inc. on Jul 21, 2010 in Monmouth Junction, NJ. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Monmouth Junction, NJ (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation