# Saipan Ice & Water Co. Inc - Inspection Records

Source: https://www.keypedia.com/companies/saipan-ice-water-co-inc/72bc5566-952b-498e-8128-bd3bcb233889

> Inspection records and compliance data for Saipan Ice & Water Co. Inc in Saipan, Northern Mariana Islands. Access full analysis and detailed observations.

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## Details

- Name: Saipan Ice & Water Co. Inc
- FEI Number: 3007744078
- City: Saipan
- State: Northern Mariana Islands
- Country Name: United States
- Address Line 1: Lower Base Drive
- Zip Code: 96950

## Related Documents

- [FDA Inspection 1238332 - Saipan Ice & Water Co. Inc - 2024-05-13](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/f2cd76e3-9507-4b4d-a07f-96c5fb01c84e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 13, 2024
- [FDA Inspection 1238332 - Saipan Ice & Water Co. Inc - 2024-05-13](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/0e26f056-fe97-4c23-a1e4-98a96d88427f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 13, 2024
- [FDA Inspection 1108395 - Saipan Ice & Water Co. Inc - 2019-09-16](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/838e7ae3-a0b2-4f39-ab15-f521df18cd3f) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2019
- [FDA Inspection 1108395 - Saipan Ice & Water Co. Inc - 2019-09-16](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/7a0b86f1-d523-436e-a856-ddd1c2fbd3cd) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2019
- [FDA Inspection 986413 - Saipan Ice & Water Co. Inc - 2016-09-13](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/1889ee17-0dc0-4fe7-8708-62b4e2547784) — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2016
- [FDA Inspection 604721 - Saipan Ice & Water Co. Inc - 2009-07-21](https://www.keypedia.com/records/fda_inspections/saipan-ice-water-co-inc/42c8cd86-d0d1-45fc-a2c5-91f32995104d) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2009

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