# FDA Inspection 855023 - Schindele Enterprises dba Midwest Wholesale - November 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/schindele-enterprises-dba-midwest-wholesale/eda73a6f-a565-4eb7-85f8-6f044ba24f68
Source feed: FDA_Inspections

> FDA Inspection 855023 for Schindele Enterprises dba Midwest Wholesale on November 05, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855023
- Company Name: Schindele Enterprises dba Midwest Wholesale
- Inspection Date: 2013-11-05
- Classification: Official Action Indicated (OAI)
- Project Area: Unapproved and Misbranded Drugs
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 907271 - 2014-12-10](https://www.keypedia.com/records/fda_inspections/schindele-enterprises-dba-midwest-wholesale/03687cb6-28c9-464c-9e5f-f4e850a16767)
- [FDA Inspection 855023 - 2013-11-05](https://www.keypedia.com/records/fda_inspections/schindele-enterprises-dba-midwest-wholesale/4bc08885-575d-4902-92cf-186e7fba6ac2)

Company: https://www.keypedia.com/companies/schindele-enterprises-dba-midwest-wholesale/82690ffd-f9d8-4a02-80c7-fa16374da71a

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c