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{
"resource_uri": "https://fragdenstaat.de/api/v1/message/641424/?format=api",
"id": 641424,
"url": "https://fragdenstaat.de/anfrage/angebot-von-pfizer-und-biontech-uber-corona-impfstoff/#nachricht-641424",
"request": "https://fragdenstaat.de/api/v1/request/213138/?format=api",
"sent": true,
"is_response": true,
"is_postal": false,
"is_draft": false,
"kind": "email",
"is_escalation": false,
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"sender_public_body": "https://fragdenstaat.de/api/v1/publicbody/16038/?format=api",
"recipient_public_body": null,
"status": null,
"timestamp": "2021-11-03T12:34:51+01:00",
"registered_mail_date": null,
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"attachments": [],
"subject": "Complaint 1690/2021/OAM",
"content": "Decision on the European Commission's failure to reply to a request for public access to documents related to the purchase of the BioNTech-Pfizer COVID-19 vaccine - GESTDEM 2021/0863\n\nDear Mr Antragsteller/in,\nYou submitted a complaint to the European Ombudsman against the European Commission about its failure to reply to your request for public access to documents concerning an offer for the purchase of COVID-19 vaccines.\nWe informed the Commission of your complaint and asked it to send you a reply. The Commission has informed us that it has sent you an initial reply to your access request on 27 October 2021.\nThe case is therefore closed with the conclusion that it has been settled.\nPlease note that this inquiry concerned exclusively the Commission's failure to reply to your correspondence. As already mentioned, if you are dissatisfied with the Commission's reply, you are entitled to make a confirmatory application (in accordance with Article 7(2) of Regulation 1049/2001<https://eur-lex.europa.eu/legal-content/EN/ALL/?uri=celex%3A32001R1049>). The Ombudsman can consider any issues related to the handling and/or substance of the access request only after a valid confirmatory application has been submitted and the statutory timelines for replying have elapsed.\nIf you decide to make a new complaint at a later stage, there is no need to resubmit the documents already included in your file. A reference to the present complaint number will suffice.\n\nYours sincerely,",
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"Decision on the European Commission's failure to reply to a request for public access to documents related to the purchase of the BioNTech-Pfizer COVID-19 vaccine - GESTDEM 2021/0863\n\nDear Mr "
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",\nYou submitted a complaint to the European Ombudsman against the European Commission about its failure to reply to your request for public access to documents concerning an offer for the purchase of COVID-19 vaccines.\nWe informed the Commission of your complaint and asked it to send you a reply. The Commission has informed us that it has sent you an initial reply to your access request on 27 October 2021.\nThe case is therefore closed with the conclusion that it has been settled.\nPlease note that this inquiry concerned exclusively the Commission's failure to reply to your correspondence. As already mentioned, if you are dissatisfied with the Commission's reply, you are entitled to make a confirmatory application (in accordance with Article 7(2) of Regulation 1049/2001<https://eur-lex.europa.eu/legal-content/EN/ALL/?uri=celex%3A32001R1049>). The Ombudsman can consider any issues related to the handling and/or substance of the access request only after a valid confirmatory application has been submitted and the statutory timelines for replying have elapsed.\nIf you decide to make a new complaint at a later stage, there is no need to resubmit the documents already included in your file. A reference to the present complaint number will suffice.\n\nYours sincerely,"
]
],
"sender": "Europäischer Bürgerbeauftragte",
"status_name": null,
"last_modified_at": "2024-01-03T16:02:23.118447+01:00"
}