FDA issued a Warning Letter to Nordimex, LLC on 10/11/2011 as a result of this inspection.
FDA investigators audited the OPMX - San Diego, CA, United States facility and issued 3 inspectional observations (via FDA 483) on 31 May 2011.
Add To Cart
- Category: Foods & Cosmetics / Human Drugs
- Number of Observations: 3
- Inspection end: 31 May 2011
- Location: San Diego, United States
- FEI: 3008937007