# Genentech, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/genentech-inc/709aa262-e8df-42fa-bec6-02673e7f52ec

> Inspection records and compliance data for Genentech, Inc. in South San Francisco, California. Access full analysis and detailed observations.

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## Details

- Name: Genentech, Inc.
- FEI Number: 2917293
- City: South San Francisco
- State: California
- Country Name: United States
- Address Line 1: 1 Dna Way Bldg 5
- Zip Code: 94080
- Facility Type: Manufacturer

## Related Documents

- [CRL - Genentech, Inc. - Unknown Date](https://www.globalkeysolutions.net/records/crl/genentech-inc/82cfc039-6c70-459b-ad38-2e0ed36626fa) — source: FDA, date: Invalid Date
- [FDA Inspection 1263573 - Genentech, Inc. - 2025-04-21](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/d1879b40-adc5-4e34-a983-95d715e0461e) — source: FDA, date: April 21, 2025
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- [FDA Inspection 1235655 - Genentech, Inc. - 2024-03-20](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/6b6012ce-24be-471f-8d57-85bb92f5fb25) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2024
- [483 - Genentech, Inc. - 2024-03-12](https://www.globalkeysolutions.net/records/483/genentech-inc/7887b305-0de6-472c-b596-8cbd94e8d300) — source: FDA, date: March 12, 2024
- [FDA Inspection 1233203 - Genentech, Inc. - 2024-03-12](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/c630a432-31f9-476d-9f0d-9c7a9ed953d0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 12, 2024
- [483 - Genentech, Inc. - 2023-08-11](https://www.globalkeysolutions.net/records/483/genentech-inc/ce85e9f0-3331-495a-b1b4-a7e2df5fa79b) — source: FDA, date: August 11, 2023
- [FDA Inspection 1214575 - Genentech, Inc. - 2023-08-11](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/84a034a5-344a-46c2-9b20-5a05a08e407b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2023
- [FDA Inspection 1200732 - Genentech, Inc. - 2023-02-21](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/810907e1-e784-4115-9e9a-3c66ad8287c7) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2023
- [483 - Genentech, Inc. - 2023-02-01](https://www.globalkeysolutions.net/records/483/genentech-inc/1cd09b7b-965e-44ed-b8cb-5c204ab45f19) — source: FDA, date: February 1, 2023
- [483 - Genentech, Inc. - 2023-01-31](https://www.globalkeysolutions.net/records/483/genentech-inc/e020acbc-f66e-4314-a8bc-c156ef8c9a94) — source: FDA, date: January 31, 2023
- [EIR - Genentech, Inc. - 2022-10-07](https://www.globalkeysolutions.net/records/eir/genentech-inc/c790563c-45ba-439c-8c24-6cd1f80fcf3f) — source: FDA, date: October 7, 2022
- [FDA Inspection 1181972 - Genentech, Inc. - 2022-10-07](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/614be98f-b337-45e8-8a85-07d35ce9cb7e) — classification: No Action Indicated (NAI), source: FDA, date: October 7, 2022
- [483 - Genentech, Inc. - 2022-05-26](https://www.globalkeysolutions.net/records/483/genentech-inc/3b630c1e-0dc5-44a8-a456-256f25c6a163) — source: FDA, date: May 26, 2022
- [FDA Inspection 1092593 - Genentech, Inc. - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/428650ca-ecaf-4186-b5cb-99e2f4b42666) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2019
- [FDA Inspection 1028664 - Genentech, Inc. - 2017-08-03](https://www.globalkeysolutions.net/records/fda_inspections/genentech-inc/4ae62f13-6320-43b7-ab45-569c03e5d13e) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2017
- [483 - Genentech, Inc. - 2011-09-27](https://www.globalkeysolutions.net/records/483/genentech-inc/18f90c1b-4f69-4c48-99f7-a22fc019324c) — source: FDA, date: September 27, 2011

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