# DO & CO Los Angeles, Inc. (DO & CO), Redondo Beach, CA – FDA Inspections

Source: https://www.keypedia.com/companies/do-co-los-angeles-inc-do-co/960a0128-071f-40b0-9766-32c9b385c1c8

> Inspection records and compliance data for DO & CO Los Angeles, Inc. (DO & CO) in Redondo Beach, California. 4 FDA inspections on record, 1 Form 483, 1 warning letter, last inspected November 06, 2024.

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## Details

- Name: DO & CO Los Angeles, Inc. (DO & CO)
- FEI Number: 3013418152
- Address Line 1: 4000 Redondo Beach Ave Ste 101
- City: Redondo Beach
- State: California
- Zip Code: 90278
- Country Name: United States
- Address: 4000 Redondo Beach Ave Ste 101, Redondo Beach, California 90278, United States
- Country: United States

## Related Documents

- [WARNING_LETTER - DO & CO Los Angeles, Inc. (DO & CO) - 2025-08-18](https://www.keypedia.com/records/warning_letter/do-co-los-angeles-inc-do-co/209bf737-ae93-41af-b5d9-40683b5fc633) — source: FDA, date: August 18, 2025
- [FDA Inspection 1253862 - DO & CO Los Angeles, Inc. (DO & CO) - 2024-11-06](https://www.keypedia.com/records/fda_inspections/do-co-los-angeles-inc-do-co/f459c4bd-91cc-4dbe-a67b-a33f7947b321) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2024
- [FDA Inspection 1117181 - DO & CO Los Angeles, Inc. (DO & CO) - 2020-02-07](https://www.keypedia.com/records/fda_inspections/do-co-los-angeles-inc-do-co/d4cbd039-deba-48eb-8186-dc07f72ade19) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2020
- FDA Inspection 1117181 - DO & CO Los Angeles, Inc. (DO & CO) - 2020-02-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2020
- [FDA Inspection 1023628 - DO & CO Los Angeles, Inc. (DO & CO) - 2017-08-28](https://www.keypedia.com/records/fda_inspections/do-co-los-angeles-inc-do-co/dc70831a-1062-40dd-a314-7772e4182c43) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2017
- FDA Inspection 1009757 - DO & CO Los Angeles, Inc. (DO & CO) - 2017-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2017

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