FDA Inspection 1145465 — WECO MANUFACTURING GROUP-HENRIETTA/ ESI
The FDA completed an inspection of WECO MANUFACTURING GROUP-HENRIETTA/ ESI on Jun 24, 2021 in Rochester, NY. 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
- Jun 24, 2021
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Rochester, NY (United States)