Home » Indian State FDA Recommends CBI Probe Into Defective Medical Device Recall Case
Indian State FDA Recommends CBI Probe Into Defective Medical Device Recall Case
The Maharashtra Food and Drug Administration has recommended that the state home department hand over the case related to Johnson & Johnson subsidiary De Puy Orthopaedics’ inappropriate recall of ASR Hip Replacement Implants in India to the Central Bureau of Investigation.
Pharmabiz.com
Pharmabiz.com
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