# OLMA-XXI INC - Inspection Records

Source: https://www.keypedia.com/companies/olma-xxi-inc/08409422-f7d7-4e96-a7b2-aa4df7ecaddf

> Inspection records and compliance data for OLMA-XXI INC in Brooklyn, New York. Access full analysis and detailed observations.

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## Details

- Name: OLMA-XXI INC
- FEI Number: 3005455359
- City: Brooklyn
- State: New York
- Country Name: United States
- Address Line 1: 204 28th St
- Zip Code: 11232

## Related Documents

- [FDA Inspection 1312078 - OLMA-XXI INC - 2026-04-10](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/3e24a5a1-ba43-482e-92b6-ce8a3cff6aba) — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2026
- [FDA Inspection 1312078 - OLMA-XXI INC - 2026-04-10](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/ca3efcea-6e31-4501-88bb-94cce6a95ab1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2026
- [FDA Inspection 1001747 - OLMA-XXI INC - 2017-02-24](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/56670655-d879-48ac-aeea-707fd65d4ceb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 24, 2017
- [FDA Inspection 911501 - OLMA-XXI INC - 2015-01-21](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/2a37c764-f3ff-426d-a3e5-edabc80486e8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2015
- [FDA Inspection 800080 - OLMA-XXI INC - 2012-09-24](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/58629202-4cd0-4770-9325-35ecc27b8adf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 24, 2012
- [FDA Inspection 648553 - OLMA-XXI INC - 2010-02-25](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/0dde6ab3-cd27-4f4d-b516-e55982a0ee77) — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2010
- [FDA Inspection 543590 - OLMA-XXI INC - 2008-10-24](https://www.keypedia.com/records/fda_inspections/olma-xxi-inc/8948f32f-fe8f-46ad-9da2-e581e2812a15) — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2008

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