FDA Inspection 949735 — PureTek Corporation
The FDA completed an inspection of PureTek Corporation on October 27, 2015 in San Fernando, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 27, 2015
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- San Fernando, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 4357 | 21 CFR 211.166(a) | Results not used for expiration dates, storage cond. |