FDA Inspection 659160 — Irenda Corporation
The FDA completed an inspection of Irenda Corporation on April 29, 2010 in Los Angeles, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 29, 2010
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Los Angeles, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1942 | 21 CFR 211.180(e) | Records reviewed annually |
| 3553 | 21 CFR 211.48(a) | Plumbing System Defects |
| 3559 | 21 CFR 211.56(a) | Sanitation--buildings not clean, free of infestation |
| 4132 | 21 CFR 589.2000(d)(1) | Protein blenders, feed manufacturers, distributors |
| 4315 | 21 CFR 211.84(d)(2) | Testing Each Component for Conformity with Specs |