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Teva Pharma Suspends Irvine Production After FDA Probe - Orange County  Business Journal
Teva Pharma Suspends Irvine Production After FDA Probe - Orange County Business Journal

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

Teva Stops Production At US Plant After FDA Concerns: Report
Teva Stops Production At US Plant After FDA Concerns: Report

Teva's struggling sterile plant hit with FDA warning letter - Skyland  Analytics
Teva's struggling sterile plant hit with FDA warning letter - Skyland Analytics

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

QUALITY SYSTEM OBSERVATION 1 Procedures describing the handling ohvritten  and oral complaints related to drug products are defic
QUALITY SYSTEM OBSERVATION 1 Procedures describing the handling ohvritten and oral complaints related to drug products are defic

FDA tells Celltrion a consultant may be in order for its troubled biologics  plant | Fierce Pharma
FDA tells Celltrion a consultant may be in order for its troubled biologics plant | Fierce Pharma

Mid 2018 – Recap of Warning Letters, Import Alerts and Non-Compliances
Mid 2018 – Recap of Warning Letters, Import Alerts and Non-Compliances

Teva confirms US FDA warning letter for Hangzhou, China API plant
Teva confirms US FDA warning letter for Hangzhou, China API plant

Teva halts output at U.S. drug plant after FDA flags concerns | Reuters
Teva halts output at U.S. drug plant after FDA flags concerns | Reuters

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

UPDATE 2-Teva halts output at U.S. drug plant after FDA flags concerns
UPDATE 2-Teva halts output at U.S. drug plant after FDA flags concerns

Biocon hit with Form 483
Biocon hit with Form 483

QUALITY SYSTEM OBSERVATION 1 Procedures describing the handling ohvritten  and oral complaints related to drug products are defic
QUALITY SYSTEM OBSERVATION 1 Procedures describing the handling ohvritten and oral complaints related to drug products are defic

FDA warning letter slams B. Braun management for persistent failures at  U.S. plant | Fierce Pharma
FDA warning letter slams B. Braun management for persistent failures at U.S. plant | Fierce Pharma

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

CTLT stock spikes as Barclays says FDA cleared site violations (NYSE:CTLT)  | Seeking Alpha
CTLT stock spikes as Barclays says FDA cleared site violations (NYSE:CTLT) | Seeking Alpha

Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional  Observations). 7/13/09 – 7/24/09
Teva Parenteral Medicines, Inc. Irvine, CA. Form 483 (Inspectional Observations). 7/13/09 – 7/24/09

Teva plant tagged with warning letter for issues making schizophrenia drug  | Fierce Pharma
Teva plant tagged with warning letter for issues making schizophrenia drug | Fierce Pharma

FDA Regulation of Promotion & Advertising -- Part 4: FDA Enforcement…
FDA Regulation of Promotion & Advertising -- Part 4: FDA Enforcement…

Teva's struggling sterile plant hit with FDA warning letter - Skyland  Analytics
Teva's struggling sterile plant hit with FDA warning letter - Skyland Analytics

The most damning FDA rebukes of the COVID era
The most damning FDA rebukes of the COVID era