FDA Inspection 855749 — ImpactLife
The FDA completed an inspection of ImpactLife on November 25, 2013 in Saint Peters, MO. 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
- November 25, 2013
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Saint Peters, MO (United States)