FDA Inspection 1027819 — Selgel Mexico SA de CV
The FDA completed an inspection of Selgel Mexico SA de CV on September 15, 2017 in Toluca De Lerdo. 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
- September 15, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Toluca De Lerdo (Mexico)