FDA FastStats: A Look Back at 2013 Medical Device 483 Observations: As we approach the end of 2014, we will take a look back at FDA‘s stats on various topics sourced from their Case for Quality initiative. The FDA believes that the following type of information will:
- Help industry improve medical device quality by sharing common observations
- Identify possible areas of emerging concern, and
- Possibly help firms avoid warning letters
Our first in the series of FDA FastStats infographics is 483 inspectional observations.
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With decades of expertise built into our quality management and regulatory compliance software, the AssurX Quality Management Software Platform helps companies maintain quality and compliance standards, streamline workflow, and better manage any enterprise. Our configurable software and understanding of users’ needs produce a unique system that easily adapts as a customer’s business evolves. AssurX is an ideal partner for regulated companies looking for better operational control and efficiency while staying compliant. To learn more, visit www.assurx.com.
Other FDA FastStats Articles:
- FDA FastStats: CDRH Shows Significant Growth in Electronic Submissions; Deadline Looming for eMDR
- FDA FastStats: A Look Back at all FDA 483 Inspectional Observations for the Fiscal Year 2014
- FDA FastStats: A Look Back at 2013 Medical Device Warning Letters with Quality System Deficiencies
- FDA FastStats: A Look Back at 2013 Medical Device 483 Observations
- FDA FastStats: Got Safe Beef? New Report Suggests the US Doesn’t
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