FDA issued a Warning Letter to Bausch & Lomb on 10/31/2006 as a result of this inspection.
FDA investigators audited the Bausch & Lomb- Greenville Solutions Plant - Greenville, SC, United States facility and issued inspectional observations (via FDA 483) on 15 May 2006.
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- Category: Medical Devices & Rad Health / Human Drugs
- Inspection end: 15 May 2006
- Location: Greenville, United States
- FEI: 1032500