FDA Inspection 813940 — Eisertech LLC

Eisertech LLC — FEI 3009381326

The FDA completed an inspection of Eisertech LLC on December 19, 2012 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 19, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures