FDA Good Manufacturing Practices
in Flow Meter Manufacturing

The FDA’s Good Manufacturing Practices (GMP) comprise a set of government regulations, codes, and guidelines for the manufacturing of drugs, medical devices, diagnostic products, foods, and active pharmaceutical ingredients. The GMP ensures safety in products by monitoring every aspect of a manufacturing process from the design of a product, to the physical production, testing, packaging, and storage of both components and finished goods. Even after the flow meter has been delivered, you can rely on our Good Manufacturing Practices: the Key Instruments commitment to GMP ensures a promptly and properly serviced product if ever necessary.

By administering and complying with FDA’s Good Manufacturing Practices, Key Instruments maintains an active quality control documentation process. This documentation tracks all aspects of the production of goods from the purchase of raw materials to final testing and sale of finished goods. The FDA monitors this documentation system with regular audits to ensure compliance. Additionally, our precise documentation system allows us to continually improve the manufacturing process, which leads to the consistent production of high quality flow meters for our customers. Key Instruments does more than adhere to GMP: we have and will continue to strive to exceed FDA guidelines for safety and quality.