FDA Inspection 1069151 — Jk Products Gmbh
The FDA completed an inspection of Jk Products Gmbh on Sep 21, 2018 in Bad Honnef. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 21, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Bad Honnef (Germany)