# Catalent Greenville Inc - Inspection Records

Source: https://www.keypedia.com/companies/catalent-greenville-inc/11f944f4-641e-45e5-9c6b-3a3a7b1ab8cd

> Inspection records and compliance data for Catalent Greenville Inc in Greenville, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: Catalent Greenville Inc
- FEI Number: 3000209735
- City: Greenville
- State: North Carolina
- Country Name: United States
- Address Line 1: 1240 Sugg Pkwy
- Zip Code: 27834
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - Catalent Greenville Inc - 2025-10-24](https://www.keypedia.com/records/483/catalent-greenville-inc/4533beac-cc6a-41f8-8d08-00ecde98205c) — source: FDA, date: October 24, 2025
- [FDA Inspection 1267356 - Catalent Greenville Inc - 2025-10-24](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/e70481ed-ec74-44fe-a523-966e8da08563) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 24, 2025
- [FDA Inspection 1231042 - Catalent Greenville Inc - 2024-01-31](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/80298d15-bf27-4477-a164-633709221058) — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2024
- [483 - Catalent Greenville Inc - 2019-07-12](https://www.keypedia.com/records/483/catalent-greenville-inc/bc6cefe3-948d-478e-9077-d2727d1b46a4) — source: FDA, date: July 12, 2019
- [FDA Inspection 1097051 - Catalent Greenville Inc - 2019-07-12](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/be367675-334c-4c75-955e-aad4e684ecfe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2019
- [FDA Inspection 1065149 - Catalent Greenville Inc - 2018-08-24](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/8d127aee-29c0-4744-adcb-d06b0dc377d6) — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2018
- [FDA Inspection 1019260 - Catalent Greenville Inc - 2017-04-13](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/8631aba9-7a96-4195-8726-7b0b6d33810b) — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- [FDA Inspection 983236 - Catalent Greenville Inc - 2016-07-14](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/a038ffd6-9cf4-4be5-ae9a-22a0e32685e4) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2016
- [EIR - Catalent Greenville Inc - 2014-05-02](https://www.keypedia.com/records/eir/catalent-greenville-inc/9108584d-1f49-4651-96c0-06c1104494b8) — source: FDA, date: May 2, 2014
- [FDA Inspection 880075 - Catalent Greenville Inc - 2014-05-02](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/a847fa0c-c5e8-44db-8335-304ad4eac500) — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2014
- [FDA Inspection 845560 - Catalent Greenville Inc - 2013-08-21](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/bda5f3b6-afd5-4e69-874b-37d54121c16c) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2013
- [FDA Inspection 781526 - Catalent Greenville Inc - 2012-05-11](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/98870512-a3fe-42e7-a29f-ee4bc8788ca5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2012
- [FDA Inspection 781692 - Catalent Greenville Inc - 2012-05-11](https://www.keypedia.com/records/fda_inspections/catalent-greenville-inc/cf524593-a856-4e76-875d-a5f4440b860a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2012

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