Home / Inspections / 979008

FDA Inspection 979008 — Andwin Scientific

Andwin Scientific — FEI 2027344

The FDA completed an inspection of Andwin Scientific on July 27, 2016 in Simi Valley, 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
July 27, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Simi Valley, CA (United States)

Facility

Other inspections at this facility

  • 1254276 (NAI Wed Oct 30 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1154346 (NAI Tue Oct 05 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 875495 (NAI Wed Apr 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 773216 (NAI Mon Mar 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources