FDA Inspection 1109013 — Paragon BioTeck Inc
The FDA completed an inspection of Paragon BioTeck Inc on September 25, 2019 in Portland, OR. 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
- September 25, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Portland, OR (United States)