FDA Inspection 1022942 — E.A. Beck & Co.
The FDA completed an inspection of E.A. Beck & Co. on August 10, 2017 in Schaumburg, IL. 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
- August 10, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Schaumburg, IL (United States)