483
Limerick IncLimerick Inc – FDA 483, Aug 15, 2025
Record Details
An FDA inspection of Limerick Inc, a medical device manufacturer in Burbank, CA, revealed three significant observations. The firm was cited for inadequate maintenance of complaint files, insufficient procedures for controlling nonconforming products, and deficiencies in establishing and maintaining device history records for Class II devices like powered breast pumps.
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ID · 99d19222-f8a2-4a36-8d1a-6025f1a02319
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