FDA Inspection 1068316 — Streck, Inc.
The FDA completed an inspection of Streck, Inc. on Sep 20, 2018 in La Vista, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- La Vista, NE (United States)