FDA Inspection 1130510 — Versiti Michigan Inc
The FDA completed an inspection of Versiti Michigan Inc on Sep 4, 2020 in Grand Rapids, MI. 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
- Sep 4, 2020
- Fiscal Year
- 2020
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Grand Rapids, MI (United States)