483
Philips Respironics, Inc.Philips Respironics, Inc. – FDA 483, Nov 9, 2021
Record Details
This FDA Form 483 report for Philips Respironics, Inc. indicates that no inspectional observations were noted during the inspection. The report therefore does not detail any specific deficiencies or violations.
- Company
- Philips Respironics, Inc.
- Inspection date
- November 9, 2021
- Product type
- device
- Office
- Human Foods Program
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ID · 45c9eb4c-757c-47bf-97da-f808aab5c64b
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