FDA issued a Warning Letter to Alere San Diego, Inc. on 10/22/2012 as a result of this inspection.
FDA investigators audited the Alere San Diego - San Diego, CA, United States facility and issued inspectional observations (via FDA 483) on 27 Jun 2012.
Product details
- Category: Medical Devices & Rad Health
- Inspection end: 27 Jun 2012
- Location: San Diego, United States
- FEI: 1000125596
