FDA Inspection 1111589 — Biowy Corporation
The FDA completed an inspection of Biowy Corporation on Nov 8, 2019 in Lake Forest, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 8, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lake Forest, CA (United States)