Abbott Diabetes Care, Inc., Alameda
Alameda
1360 S Loop Rd
Alameda, CA, 94502
United States
City | Country | Type | Project Area | Classification | Date |
---|---|---|---|---|---|
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | NAI | 11/16/23 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | NAI
; VAI | 04/21/22 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | NAI | 04/29/21 |
Alameda, CA | United States | Devices | Bioresearch Monitoring | NAI | 07/19/18 |
Alameda, CA | United States | Devices | Bioresearch Monitoring
; Compliance: Devices ; Postmarket Assurance: Devices | NAI
; VAI | 12/04/17 |
Alameda, CA | United States | 10/13/17 | |||
Alameda, CA | United States | 10/21/16 | |||
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | NAI | 03/10/16 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | VAI | 10/22/15 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | NAI
; VAI | 02/07/14 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | OAI | 05/31/13 |
Alameda, CA | United States | Devices | Compliance: Devices | NAI | 07/24/12 |
Alameda, CA | United States | Devices | Compliance: Devices
; Postmarket Assurance: Devices | OAI | 03/05/10 |
Alameda, CA | United States | Devices | Bioresearch Monitoring
; Compliance: Devices ; Postmarket Assurance: Devices | VAI | 03/13/09 |
Alameda, CA | United States | 02/29/08 | |||
Alameda, CA | United States | 03/13/07 | |||
Alameda, CA | United States | 10/20/06 | |||
Alameda, CA | United States | 06/16/06 | |||
Alameda, CA | United States | 09/01/05 | |||
Alameda, CA | United States | 04/16/04 | |||
Alameda, CA | United States | 02/18/04 | |||
Alameda, CA | United States | 11/14/03 | |||
Alameda, CA | United States | 05/25/01 |
Reference: FDA Data Dashboard
Note: There are 23 inspections, but 24 FDA Data Dashboard records. This is because the agency enumerates inspection-classifications, not inspection events.