# Cetro America Inc. - Inspection Records

Source: https://www.keypedia.com/companies/cetro-america-inc/425c796a-3b5b-4618-a7e4-03649bb4ba5e

> Inspection records and compliance data for Cetro America Inc. in Meriden, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Cetro America Inc.
- FEI Number: 3004167720
- City: Meriden
- State: Connecticut
- Country Name: United States
- Address Line 1: 33 Charles St
- Zip Code: 06450

## Related Documents

- [FDA Inspection 1331974 - Cetro America Inc. - 2026-08-21](https://www.keypedia.com/records/fda_inspections/cetro-america-inc/d14180be-e587-479d-817c-bb91f0b20994) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 21, 2026
- [483 - Cetro America Inc. - 2024-02-01](https://www.keypedia.com/records/483/cetro-america-inc/313ac8a5-1fde-487c-92e5-9c8506d70b0c) — source: FDA, date: February 1, 2024
- [FDA Inspection 1228667 - Cetro America Inc. - 2024-02-01](https://www.keypedia.com/records/fda_inspections/cetro-america-inc/53dcf925-ee9b-4a22-a6d8-d46236f3e107) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 1, 2024
- [FDA Inspection 1228667 - Cetro America Inc. - 2024-02-01](https://www.keypedia.com/records/fda_inspections/cetro-america-inc/a0d9b330-6838-46bb-b417-801d336d2dbd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 1, 2024
- [FDA Inspection 1081731 - Cetro America Inc. - 2019-02-27](https://www.keypedia.com/records/fda_inspections/cetro-america-inc/d3dc3908-602e-4c46-8f5f-2bc8aa7de250) — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2019
- [483 - Cetro America Inc. - 2018-01-11](https://www.keypedia.com/records/483/cetro-america-inc/40797fe8-5154-4c8c-bf7e-236f3609c5ad) — source: FDA, date: January 11, 2018
- [FDA Inspection 1038035 - Cetro America Inc. - 2018-01-11](https://www.keypedia.com/records/fda_inspections/cetro-america-inc/d2336594-837f-45ff-90ab-85fe27d77a46) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 11, 2018

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