FDA Inspection 899317 — ProMed Pharma, LLC
The FDA completed an inspection of ProMed Pharma, LLC on Oct 6, 2014 in Plymouth, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 6, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Plymouth, MN (United States)
Additional Details
Postmarket Audit Inspections