# Ozark Bottling, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ozark-bottling-llc/9f67858a-116d-4d95-8255-cd046e53d43e

> Inspection records and compliance data for Ozark Bottling, LLC in Lake Ozark, Missouri. Access full analysis and detailed observations.

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## Details

- Name: Ozark Bottling, LLC
- FEI Number: 3001584349
- City: Lake Ozark
- State: Missouri
- Country Name: United States
- Address Line 1: 3468 Old Highway 54
- Zip Code: 65049

## Related Documents

- [FDA Inspection 1099961 - Ozark Bottling, LLC - 2019-08-12](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/d4520018-7981-4342-a1c7-c01821c42fbb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 12, 2019
- [FDA Inspection 1012938 - Ozark Bottling, LLC - 2017-04-10](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/f765c2d7-6acc-4e81-8222-4d3cb8406fb2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2017
- [FDA Inspection 839662 - Ozark Bottling, LLC - 2013-07-02](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/713c7751-04ab-4fab-9989-46c9eec3275e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2013
- [FDA Inspection 759270 - Ozark Bottling, LLC - 2011-12-09](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/e7c1de8d-44ba-477e-af65-e20186d0fc02) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 9, 2011
- [FDA Inspection 710958 - Ozark Bottling, LLC - 2011-02-08](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/9ab82d00-538d-46d8-8900-9ece6e84b9b5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2011
- [FDA Inspection 644644 - Ozark Bottling, LLC - 2009-11-12](https://www.globalkeysolutions.net/records/fda_inspections/ozark-bottling-llc/05a9b058-e3d9-4db6-9f02-e8fd617e10ed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 12, 2009

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