FDA Inspection 1090194 — Radnostix

Radnostix — FEI 3003350319

The FDA completed an inspection of Radnostix on May 10, 2019 in Idaho Falls, ID. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Idaho Falls, ID (United States)