FDA Inspection 1221437 — Lumicell, Inc.
The FDA completed an inspection of Lumicell, Inc. on October 16, 2023 in Newton, 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
- October 16, 2023
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Newton, MA (United States)