FDA issued a Warning Letter to Entellus Medical on 4/6/2017 as a result of this inspection.
FDA investigators audited the Entellus Medical - Plymouth, MN, United States facility and issued inspectional observations (via FDA 483) on 27 Sep 2016.
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- Category: Medical Devices & Rad Health
- Inspection end: 27 Sep 2016
- Location: Plymouth, United States
- FEI: 3006345872