FDA Inspection 593351 — Ram Precision, Inc.

Ram Precision, Inc. — FEI 3005004799

The FDA completed an inspection of Ram Precision, Inc. on June 22, 2009 in Centerville, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Centerville, OH (United States)