FDA issued a Warning Letter to Huestis Machine Corporation on 8/6/2013 as a result of this inspection.
FDA investigators audited the Huestis Machine - Bristol, RI, United States facility and issued 9 inspectional observations (via FDA 483) on 13 May 2013.
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- Category: Medical Devices & Rad Health
- Number of Observations: 9
- Inspection end: 13 May 2013
- Location: Bristol, United States
- FEI: 1219183