FDA issued a Warning Letter to Conair Corporation on 8/12/2013 as a result of this inspection.
FDA investigators audited the Conair - Stamford, CT, United States facility and issued 8 inspectional observations (via FDA 483) on 31 May 2013.
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- Category: Medical Devices & Rad Health
- Number of Observations: 8
- Inspection end: 31 May 2013
- Location: Stamford, United States
- FEI: 1000121041