483 RESPONSE
Whole Foods Market Group Inc.Whole Foods Market Group Inc. – FDA 483 Response, Feb 18, 2016
Record Details
This 483 RESPONSE record concerns Whole Foods Market Group Inc., with an inspection on February 18, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection date
- February 18, 2016
- Product type
- Devices
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ID · bea2d9a0-951c-4de4-ad0a-4f4aa087298a
Violation Codes1
21 CFR 173.315(a)(5)
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