FDA issued a Warning Letter to TreyMed, Inc. on 1/9/2015 as a result of this inspection.
FDA investigators audited the Treymed - Sussex, WI, United States facility and issued 6 inspectional observations (via FDA 483) on 21 Oct 2014.
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- Category: Medical Devices & Rad Health
- Number of Observations: 6
- Inspection end: 21 Oct 2014
- Location: Sussex, United States
- FEI: 3003007937