FDA issued a Warning Letter to Teleflex Medical on 3/11/2014 as a result of this inspection.
483 Teleflex Medical Sep 2013
483 Teleflex Medical Sep 2013Nicole Williams FDA$119.00 - Available Now
FDA investigators audited the Teleflex Medical - Arlington Heights, IL, United States facility and issued 5 inspectional observations (via FDA 483) on 24 Sep 2013.
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- Category: Medical Devices & Rad Health
- Number of Observations: 5
- Inspection end: 24 Sep 2013
- Location: Arlington Heights, United States
- FEI: 1417411