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483
•Darmerica, LLC•March 11, 2022

Darmerica, LLC – FDA 483, Mar 11, 2022

Record Details

Darmerica, LLC, a human and animal API repacker/relabeler in Casselberry, Florida, was cited for significant deficiencies across its quality system. Observations included inadequate supplier qualification and COA verification, improper storage of APIs, deficient controls for analytical equipment, failure to follow annual product review procedures, and inadequate cleaning procedures. These issues indicate a lack of robust quality control and adherence to established protocols.

Company
Darmerica, LLC
Inspection date
March 11, 2022
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
Person
  • Nicole E. Knowlton (Investigator )
View Company Profile

ID · b8e293c0-3ea7-4303-8802-e0b9f47fbf02

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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