FDA Inspection 602577 — Jedmed Instrument Company

Jedmed Instrument Company — FEI 1926681

The FDA completed an inspection of Jedmed Instrument Company on July 30, 2009 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)