FDA Inspection 1172085 — ImpactLife

ImpactLife — FEI 1970361

The FDA completed an inspection of ImpactLife on May 18, 2022 in Ottumwa, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 18, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Ottumwa, IA (United States)