FDA Inspection 855023 — Schindele Enterprises dba Midwest Wholesale
The FDA completed an inspection of Schindele Enterprises dba Midwest Wholesale on November 5, 2013 in Nixa, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 3 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- November 5, 2013
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Unapproved and Misbranded Drugs
- Location
- Nixa, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15641 | 21 CFR 111.453 | Written procedures - holding |
| 15652 | 21 CFR 111.465(b) | Retain reserve samples - 1 year, 2 years |
| 15658 | 21 CFR 111.475(a) | Records - holding, distribution: readily available |