FDA Inspection 1034515 — Streck, Inc.

Streck, Inc. — FEI 1950302

The FDA completed an inspection of Streck, Inc. on Nov 10, 2017 in La Vista, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 10, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
La Vista, NE (United States)