The Food and Drug Administration completed an inspection of Parter Medical Products, Inc. in Carson on Feb. 13, according to information published on the FDA’s website.
Agency officials reviewed the following topics during the visit:
- Compliance: Devices
- Postmarket Assurance: Devices
The inspection report concluded that Parter Medical Products, Inc. is not required to take corrective actions regarding the company’s management operations.
The FDA conducts regular facility inspections across the country to assess compliance with FDA-regulated standards and laws intended to protect public health. Summaries of inspection findings are made publicly available.
Information from the agency’s website describes the FDA as a government authority overseeing the safety and quality of drugs for humans and animals, biological items, medical products and tobacco through monitoring of manufacturing and distribution.
Details for this article were sourced from the U.S. Food and Drug Administration. The original data set can be accessed here.
