FDA Inspection 1024977 — M.E.E.I. Boston Keratoprosthesis
The FDA completed an inspection of M.E.E.I. Boston Keratoprosthesis on July 25, 2017 in Boston, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 25, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boston, MA (United States)