483 Roundup: FDA Hits Six Firms for Quality Lapses
The FDA cited six devicemakers for a range of GMP and other failures, including root-cause analysis for nonconforming products and lax environmental controls.
Source: The GMP Letter
The FDA cited six devicemakers for a range of GMP and other failures, including root-cause analysis for nonconforming products and lax environmental controls.
Source: The GMP Letter