# The Natural Fruit and Beverage Co. Ltd. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/the-natural-fruit-and-beverage-co-ltd/c3f45d81-a225-4fd7-8516-fb5f2f23706c

> Inspection records and compliance data for The Natural Fruit and Beverage Co. Ltd. in Coatbridge, None. Access full analysis and detailed observations.

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## Details

- Name: The Natural Fruit and Beverage Co. Ltd.
- FEI Number: 3008132375
- City: Coatbridge
- State: None
- Country Name: United Kingdom
- Address Line 1: Viewfield Park, Viewfield Road
- Zip Code: None

## Related Documents

- [FDA Inspection 1177760 - The Natural Fruit and Beverage Co. Ltd. - 2022-08-18](https://www.globalkeysolutions.net/records/fda_inspections/the-natural-fruit-and-beverage-co-ltd/a4028bb9-d633-40ab-8c98-2e58ca0a1170) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2022
- [FDA Inspection 1177760 - The Natural Fruit and Beverage Co. Ltd. - 2022-08-18](https://www.globalkeysolutions.net/records/fda_inspections/the-natural-fruit-and-beverage-co-ltd/dfeb1291-4b84-47e4-95b9-d30a01245c07) — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2022
- [FDA Inspection 1015807 - The Natural Fruit and Beverage Co. Ltd. - 2017-06-27](https://www.globalkeysolutions.net/records/fda_inspections/the-natural-fruit-and-beverage-co-ltd/9d3ade01-e7fd-4f59-b44b-b35e8518cceb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 27, 2017
- [FDA Inspection 1015807 - The Natural Fruit and Beverage Co. Ltd. - 2017-06-27](https://www.globalkeysolutions.net/records/fda_inspections/the-natural-fruit-and-beverage-co-ltd/15bfc9ea-64f6-462f-9401-6d6bb24e0975) — classification: No Action Indicated (NAI), source: FDA, date: June 27, 2017
- [FDA Inspection 754000 - The Natural Fruit and Beverage Co. Ltd. - 2011-10-14](https://www.globalkeysolutions.net/records/fda_inspections/the-natural-fruit-and-beverage-co-ltd/1354e3a1-0552-43a9-a445-00454ac40e7e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 14, 2011

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