# Cerovene Inc. - Inspection Records

Source: https://www.keypedia.com/companies/cerovene-inc/f23e944b-ef46-45b3-8177-af154b404c08

> Inspection records and compliance data for Cerovene Inc. in Valley Cottage, New York. Access full analysis and detailed observations.

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## Details

- Name: Cerovene Inc.
- FEI Number: 3005890568
- City: Valley Cottage
- State: New York
- Country Name: United States
- Address Line 1: 612 Corporate Way Ste 10
- Zip Code: 10989
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [FDA Inspection 1308838 - Cerovene Inc. - 2026-03-23](https://www.keypedia.com/records/fda_inspections/cerovene-inc/05d833d9-e79d-4941-8baa-1d08d52b23af) — source: FDA, date: March 23, 2026
- [FDA Inspection 1308838 - Cerovene Inc. - 2026-03-23](https://www.keypedia.com/records/fda_inspections/cerovene-inc/ec3e0746-1f62-462a-af07-047cf1e76e33) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2026
- [483 - Cerovene Inc. - 2025-04-28](https://www.keypedia.com/records/483/cerovene-inc/50422e78-6590-4f95-8c68-97fbdcd069c6) — source: FDA, date: April 28, 2025
- [483 - Cerovene Inc. - 2025-04-28](https://www.keypedia.com/records/483/cerovene-inc/184d7a73-cf0a-4331-9574-441718afd839) — source: FDA, date: April 28, 2025
- [FDA Inspection 1269142 - Cerovene Inc. - 2025-04-28](https://www.keypedia.com/records/fda_inspections/cerovene-inc/ca8c9d19-4154-4d01-97d9-b1defafb20b3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2025
- [FDA Inspection 1215341 - Cerovene Inc. - 2023-08-01](https://www.keypedia.com/records/fda_inspections/cerovene-inc/bb14bb94-6bdf-4b86-9bd0-0d8ff92ef29d) — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2023
- [FDA Inspection 1074159 - Cerovene Inc. - 2018-11-05](https://www.keypedia.com/records/fda_inspections/cerovene-inc/9f74c709-84da-4852-ac10-55da084f60f1) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2018
- [FDA Inspection 1001439 - Cerovene Inc. - 2017-02-08](https://www.keypedia.com/records/fda_inspections/cerovene-inc/afe846b8-4499-4b93-bb15-856205fe84e6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2017
- [FDA Inspection 924812 - Cerovene Inc. - 2015-05-04](https://www.keypedia.com/records/fda_inspections/cerovene-inc/ccc2b08f-598d-4264-89cd-3d6b5452e8d0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2015
- [FDA Inspection 852062 - Cerovene Inc. - 2013-10-15](https://www.keypedia.com/records/fda_inspections/cerovene-inc/8c8bb957-2177-4313-9f20-9d1e144db55c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2013
- [FDA Inspection 800745 - Cerovene Inc. - 2012-09-20](https://www.keypedia.com/records/fda_inspections/cerovene-inc/9f4f8d7a-9151-4f73-8d64-409b83172de7) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2012
- [FDA Inspection 713105 - Cerovene Inc. - 2011-03-08](https://www.keypedia.com/records/fda_inspections/cerovene-inc/04350242-a22e-4e3a-8c7a-0d628d9a8e75) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2011

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