The Food and Drug Administration (FDA) conducted an inspection at AR Fabricating in Georgetown on Feb. 11, as detailed in information available on the FDA’s website.
The resulting report stated that AR Fabricating needs to address management procedures related to device compliance. There were no required corrections in the other evaluated area.
The FDA regularly inspects facilities nationwide to assess whether workplaces and their products meet all FDA-enforced laws and regulations aimed at safeguarding public health. Findings from inspections are made available to the public.
The agency’s website describes the FDA as a federal organization charged with overseeing the safety and quality of human and animal drugs, biological products, medical devices and tobacco products.
Information for this report comes from the U.S. Food and Drug Administration. The original source data is available here.
