Facet's QUALITY management system is dedicated to consistently provide products that meet or exceed customer and regulatory requirements.
- Our Quality Management Team is involved in every step
of quality throughout the product lifecycle.
- Quality Control for incoming components, in process
inspection, and finished goods.
- Quality Assurance for testing and validation of design
- Establishment of sampling plans for inspection and testing.
- Facet conducts internal audits at planned intervals to
ensure the quality management system is effective.
- Facet rigorously follows the requirements outlined in
21 CFR 820, the US Food and Drug Administration's
Quality System Regulation (QSR).
Facet Technologies is committed to meeting customer and regulatory requirements and enhancing internal and external customer satisfaction through continual improvement of our products, services, quality management system, and a dedication to its core values.
- ISO 13485 Certification
- FDA Registered
- Medical Device Directive 93/42/EEC including Annex II
- ISO 13485 Health Canada Certification
File: 13485 Exp June 9 2015 CA.pdf
File: 93 42 EEC Exp June 9 2017.pdf
File: 13485 Exp June 9 2015.pdf