483
ATMOS MedizinTechnik GmbH & Co. KGATMOS MedizinTechnik GmbH & Co. KG – FDA 483, Feb 7, 2025
Record Details
This FDA Form 483 was issued to ATMOS MedizinTechnik GmbH & Co. KG. The provided document context does not detail any specific inspectional observations or deficiencies. The report indicates it was processed under a FOIA request.
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