FDA Inspection 637232 — Minneapolis Oxygen Company

Minneapolis Oxygen Company — FEI 2129790

The FDA completed an inspection of Minneapolis Oxygen Company on Jan 6, 2010 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 6, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Minneapolis, MN (United States)