FDA Inspection 933388 — Allermed Laboratories, Inc.
The FDA completed an inspection of Allermed Laboratories, Inc. on July 13, 2015 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 13, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- San Diego, CA (United States)