FDA Inspection 1009766 — Matech Inc
The FDA completed an inspection of Matech Inc on April 18, 2017 in Sylmar, CA. 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
- April 18, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sylmar, CA (United States)