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The CA provides that APS operates a facility (“Facility”) in Easton, Maryland, whose operations include:
Chemical mixing
Manufacturing of hand sanitizers, vitamin B12, and nasal inhalers
Turnkey packaging, repackaging and manufacturing solutions for the pharmaceutical, dietary supplements, animal health, consumer health, and medical device markets
The Facility is stated to be a generator of solid waste and hazardous waste. It is further stated to be engaged in the temporary storage of certain waste in containers.
EPA is stated to have conducted a Compliance Evaluation Inspection (“CEI”) at the Facility on April 25, 2018. Further, EPA is stated to have sent a Request to Show Cause and Request for Information Letter to APS on December 4, 2019, providing the company an opportunity to furnish additional information relating to compliance with applicable hazardous waste regulation. Such information is stated to have been provided EPA subsequent to December 4 ....

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