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FDA Warning Letters: May 2023 Edition
FDA Warning Letters: May 2023 Edition

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

FDA Form 483 and Warning Letter, How do differ from each other? -
FDA Form 483 and Warning Letter, How do differ from each other? -

Cipla Plant Gets FDA Warning Letter :: Generics Bulletin
Cipla Plant Gets FDA Warning Letter :: Generics Bulletin

Copaxone Warning Letter OPDP
Copaxone Warning Letter OPDP

UPDATED: Teva's struggling sterile plant hit with FDA warning letter | Fierce Pharma
UPDATED: Teva's struggling sterile plant hit with FDA warning letter | Fierce Pharma

Fake FDA warning letter scam - The Niche
Fake FDA warning letter scam - The Niche

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 recalls US-made drugs following contamination fears - The Boston Globe
Teva recalls US-made drugs following contamination fears - The Boston Globe

FDA Approval Letter - Teva Pharmaceuticals
FDA Approval Letter - Teva Pharmaceuticals

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 warning letter - IPQ
FDA warning letter - IPQ

A Harmonized Approach to Data Integrity - BioProcess InternationalBioProcess International
A Harmonized Approach to Data Integrity - BioProcess InternationalBioProcess International

FDA warns Integra LifeSciences over endotoxin testing, complaint investigations | RAPS
FDA warns Integra LifeSciences over endotoxin testing, complaint investigations | RAPS

Celltrion FDA warning causes headache for Teva's biologics ambition
Celltrion FDA warning causes headache for Teva's biologics ambition

Mid 2018 – Recap of Warning Letters, Import Alerts and Non-Compliances – gr-cis.com
Mid 2018 – Recap of Warning Letters, Import Alerts and Non-Compliances – gr-cis.com

Mid-2017 Recap of FDA Warning Letters, Import Alerts & EU Non-Compliances | Radio Compass Blog
Mid-2017 Recap of FDA Warning Letters, Import Alerts & EU Non-Compliances | Radio Compass Blog

FDA WARNS CONSUMERS ABOUT COUNTERFEIT VERSION OF TEVA'S ADDERALL | East County Magazine
FDA WARNS CONSUMERS ABOUT COUNTERFEIT VERSION OF TEVA'S ADDERALL | East County Magazine

FDA Warning Letter & Inspection Observation Trends [Updated 2023]
FDA Warning Letter & Inspection Observation Trends [Updated 2023]

Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride Injection USP 5 mg/5 mL Due to the Presence of Particulate Matter | FDA
Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride Injection USP 5 mg/5 mL Due to the Presence of Particulate Matter | FDA

UPDATED: Pii produced products recalled by Teva | Fierce Pharma
UPDATED: Pii produced products recalled by Teva | Fierce Pharma

Teva Parenterals Medicines, Inc. 12/11/09
Teva Parenterals Medicines, Inc. 12/11/09

Summary of FDA Advertising and Promotion Enforcement Activities
Summary of FDA Advertising and Promotion Enforcement Activities

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

Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd. 4/5/17
Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd. 4/5/17

Another FDA Warning Letter For Inadequate CAPAs - ECA Academy | PDF | Food And Drug Administration | Pharmaceutical Industry
Another FDA Warning Letter For Inadequate CAPAs - ECA Academy | PDF | Food And Drug Administration | Pharmaceutical Industry