FDA Inspection 1032352 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on October 9, 2017 in Temple Terrace, FL. 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
- October 9, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Temple Terrace, FL (United States)