FDA Inspection 667384 — Rotech

Rotech — FEI 3000209806

The FDA completed an inspection of Rotech on Jun 8, 2010 in Kirksville, MO. 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
Jun 8, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kirksville, MO (United States)