FDA Inspection 1026192 — ImpactLife
The FDA completed an inspection of ImpactLife on Jul 18, 2017 in Urbana, IL. 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
- Jul 18, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Urbana, IL (United States)