FDA Inspection 832479 — Matech Inc

Matech Inc — FEI 2022626

The FDA completed an inspection of Matech Inc on May 10, 2013 in Sylmar, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 10, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sylmar, CA (United States)

Citations

IDCFRDescription
315921 CFR 820.184DHR content
369621 CFR 820.100(b)Documentation