FDA Inspection 853221 — Tedor Pharma, Inc.
The FDA completed an inspection of Tedor Pharma, Inc. on October 29, 2013 in Cumberland, RI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 29, 2013
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Cumberland, RI (United States)