# Greiner Bio-One North America, Inc., Monroe, NC – FDA Inspections

Source: https://www.keypedia.com/companies/greiner-bio-one-north-america-inc/5aa9ea16-ad85-4f85-9b30-efc0ae9b36de

> Inspection records and compliance data for Greiner Bio-One North America, Inc. in Monroe, North Carolina. 7 FDA inspections on record (1 OAI), 1 Form 483, 1 warning letter, last inspected September 14, 2023.

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## Details

- Name: Greiner Bio-One North America, Inc.
- FEI Number: 3001451379
- Address Line 1: 4238 Capital Dr
- City: Monroe
- State: North Carolina
- Zip Code: 28110
- Country Name: United States
- Address: 4238 Capital Dr, Monroe, North Carolina 28110, United States
- Country: United States

## Related Documents

- FDA Inspection 1222303 - Greiner Bio-One North America, Inc. - 2023-09-14 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2023
- FDA Inspection 1222303 - Greiner Bio-One North America, Inc. - 2023-09-14 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2023
- [EIR - Greiner Bio-One North America, Inc. - 2021-10-29](https://www.keypedia.com/records/eir/greiner-bio-one-north-america-inc/1acb64d1-1c81-4f1e-a086-02f584c82841) — source: FDA, date: October 29, 2021
- [483 - Greiner Bio-One North America, Inc. - 2021-10-29](https://www.keypedia.com/records/483/greiner-bio-one-north-america-inc/d4c755b6-4e0b-4e58-b9c7-77a8b9ec9342) — source: FDA, date: October 29, 2021
- [FDA Inspection 1155664 - Greiner Bio-One North America, Inc. - 2021-10-29](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/99c892db-61ca-4cac-87a2-3fefadc27d6b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2021
- [EIR - Greiner Bio-One North America, Inc. - 2019-12-13](https://www.keypedia.com/records/eir/greiner-bio-one-north-america-inc/76af0a51-5c4c-4106-a6a4-2e23df012fc3) — source: FDA, date: December 13, 2019
- [483 - Greiner Bio-One North America, Inc. - 2019-12-13](https://www.keypedia.com/records/483/greiner-bio-one-north-america-inc/ad34488d-2369-44a6-b972-117854ce1696) — source: FDA, date: December 13, 2019
- [WARNING_LETTER - Greiner Bio-One North America, Inc. - 2019-12-13](https://www.keypedia.com/records/warning_letter/greiner-bio-one-north-america-inc/848b37fb-a03b-41e1-ad3a-e115f7d9eaf5) — source: FDA, date: December 13, 2019
- FDA Inspection 1114241 - Greiner Bio-One North America, Inc. - 2019-12-13 — classification: Official Action Indicated (OAI), source: FDA, date: December 13, 2019
- [FDA Inspection 1114241 - Greiner Bio-One North America, Inc. - 2019-12-13](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/9d28f95a-1841-4858-986f-d6c3d519afb7) — classification: Official Action Indicated (OAI), source: FDA, date: December 13, 2019
- [FDA Inspection 1021970 - Greiner Bio-One North America, Inc. - 2017-08-17](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/2d737c82-b54c-4dca-b236-3358f90507fe) — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2017
- FDA Inspection 1021970 - Greiner Bio-One North America, Inc. - 2017-08-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 17, 2017
- [FDA Inspection 843981 - Greiner Bio-One North America, Inc. - 2013-07-24](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/e2c4f6df-eb67-4054-90a5-5c80eb823cc0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2013
- FDA Inspection 843981 - Greiner Bio-One North America, Inc. - 2013-07-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2013
- FDA Inspection 703137 - Greiner Bio-One North America, Inc. - 2010-12-07 — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2010

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