# Fermic S.A. de C.V., Ciudad De Mexico, Mexico – FDA Inspections

Source: https://www.keypedia.com/companies/fermic-sa-de-cv/4a4a3a3a-7ef9-4af0-a261-beb860dde6c9

> Inspection records and compliance data for Fermic S.A. de C.V. in Ciudad De Mexico. 5 FDA inspections on record, last inspected December 13, 2024.

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## Details

- Name: Fermic S.A. de C.V.
- FEI Number: 3002806980
- Business Operations: API MANUFACTURE
- Address Line 1: Reforma No. 873, Col. San Nicolas Tolentino, Iztapalapa
- City: Ciudad De Mexico
- Country Name: Mexico
- Address: Reforma No. 873, Col. San Nicolas Tolentino, Iztapalapa, Ciudad De Mexico, Mexico
- Country: Mexico

## Related Documents

- [EIR - Fermic S.A. de C.V. - 2024-12-13](https://www.keypedia.com/records/eir/fermic-sa-de-cv/3286cbc9-aa39-4c47-baa3-b5948b02be33) — source: FDA, date: December 13, 2024
- [FDA Inspection 1258620 - Fermic S.A. de C.V. - 2024-12-13](https://www.keypedia.com/records/fda_inspections/fermic-sa-de-cv/ebea25c7-b890-4cf5-9b7e-2330781553eb) — source: FDA, date: December 13, 2024
- FDA Inspection 1258620 - Fermic S.A. de C.V. - 2024-12-13 — source: FDA, date: December 13, 2024
- FDA Inspection 1258620 - Fermic S.A. de C.V. - 2024-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2024
- FDA Inspection 1258620 - Fermic S.A. de C.V. - 2024-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2024
- FDA Inspection 1123651 - Fermic S.A. de C.V. - 2020-03-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2020
- FDA Inspection 983385 - Fermic S.A. de C.V. - 2016-07-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 22, 2016
- FDA Inspection 900001 - Fermic S.A. de C.V. - 2014-09-22 — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2014
- FDA Inspection 900001 - Fermic S.A. de C.V. - 2014-09-22 — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2014
- FDA Inspection 732883 - Fermic S.A. de C.V. - 2011-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2011

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