FDA Inspection 1100800 — Kinetic Instruments, Inc.
The FDA completed an inspection of Kinetic Instruments, Inc. on August 14, 2019 in Bethel, CT. 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
- August 14, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bethel, CT (United States)