FDA Inspection 1083568 — Mark E. Magee

Mark E. Magee — FEI 3015092481

The FDA completed an inspection of Mark E. Magee on March 15, 2019 in Lenexa, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 15, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Lenexa, KS (United States)

Additional Details

Clinical Investigator (CI)