FDA Inspection 1040052 — Ruhof Corporation
The FDA completed an inspection of Ruhof Corporation on October 18, 2017 in Mineola, NY. 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 18, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mineola, NY (United States)