# A- Z Essential Pharmaceutical, Inc., Pomona, CA – FDA Inspections

Source: https://www.keypedia.com/companies/a-z-essential-pharmaceutical-inc/c9a8e6db-9cc5-4a04-bfde-ebfe16d416fe

> Inspection records and compliance data for A- Z Essential Pharmaceutical, Inc. in Pomona, California. 4 FDA inspections on record (1 OAI), 1 Form 483, 1 warning letter, last inspected September 16, 2026.

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## Details

- Name: A- Z Essential Pharmaceutical, Inc.
- FEI Number: 3004843655
- Address Line 1: 1906 W Holt Ave
- City: Pomona
- State: California
- Zip Code: 91768
- Country Name: United States
- Address: 1906 W Holt Ave, Pomona, California 91768, United States
- Country: United States

## Related Documents

- [FDA Inspection 1336076 - A- Z Essential Pharmaceutical, Inc. - 2026-09-16](https://www.keypedia.com/records/fda_inspections/a-z-essential-pharmaceutical-inc/bc18bac5-5973-4bc2-9c23-782497c1d9ab) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2026
- FDA Inspection 1336076 - A- Z Essential Pharmaceutical, Inc. - 2026-09-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2026
- [FDA Inspection 1155221 - A- Z Essential Pharmaceutical, Inc. - 2021-10-19](https://www.keypedia.com/records/fda_inspections/a-z-essential-pharmaceutical-inc/91d76799-c7d0-4703-857f-c5f26d913837) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2021
- [WARNING_LETTER - A- Z Essential Pharmaceutical, Inc. - 2019-10-17](https://www.keypedia.com/records/warning_letter/a-z-essential-pharmaceutical-inc/862dfc6a-02da-432d-8e09-bb26761dd244) — source: FDA, date: October 17, 2019
- [FDA Inspection 1106964 - A- Z Essential Pharmaceutical, Inc. - 2019-10-17](https://www.keypedia.com/records/fda_inspections/a-z-essential-pharmaceutical-inc/6eaa4cd2-9a27-44f2-9fb7-6948915685da) — classification: Official Action Indicated (OAI), source: FDA, date: October 17, 2019
- FDA Inspection 978791 - A- Z Essential Pharmaceutical, Inc. - 2016-06-07 — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2016

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