FDA Inspection 1008076 — Sanford L.P.
The FDA completed an inspection of Sanford L.P. on Mar 24, 2017 in Downers Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 24, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Downers Grove, IL (United States)