FDA Inspection 1205661 — ImpactLife

ImpactLife — FEI 3009588529

The FDA completed an inspection of ImpactLife on May 17, 2023 in Cedar Rapids, IA. 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
May 17, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Cedar Rapids, IA (United States)