FDA Inspection 839434 — Streck, Inc.

Streck, Inc. — FEI 1950302

The FDA completed an inspection of Streck, Inc. on Jul 11, 2013 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
Jul 11, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
La Vista, NE (United States)