FDA Inspection 1024609 — Kerma Medical Products, Inc
The FDA completed an inspection of Kerma Medical Products, Inc on July 7, 2017 in Suffolk, VA. 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 7, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Suffolk, VA (United States)