www.fdanews.com/articles/139152-fda-hands-watson-483-for-batch-investigation-facility-issues
FDA Hands Watson 483 for Batch Investigation, Facility Issues
August 11, 2011
Fort Lauderdale, Fla.-based Watson Laboratories has received an FDA Form 483 after failing to thoroughly review any unexplained discrepancies or failures of batches.
Drug GMP Report
Drug GMP Report